<?xml version="1.0" encoding="utf-8"?>
<!DOCTYPE trials [
<!ELEMENT trials (trial+)>

<!ELEMENT trial (main,contacts,countries,criteria,health_condition_code,health_condition_keyword,intervention_code,
          intervention_keyword,primary_outcome,secondary_outcome,secondary_sponsor,secondary_ids,source_support,ethics_reviews)>

<!ELEMENT main (trial_id,utrn?,reg_name,date_registration,primary_sponsor,public_title,acronym?,scientific_title,scientific_acronym?,
          date_enrolment,type_enrolment,target_size,recruitment_status,url?,study_type,study_design,phase,hc_freetext?,i_freetext?,results_actual_enrolment,results_date_completed,results_url_link,results_summary,           results_date_posted,results_date_first_publication,results_baseline_char,results_participant_flow,results_adverse_events,results_outcome_measures,results_url_protocol,results_IPD_plan, results_IPD_description)>
<!ELEMENT trial_id (#PCDATA)>
<!ELEMENT utrn (#PCDATA)>
<!ELEMENT reg_name (#PCDATA)>
<!ELEMENT date_registration (#PCDATA)><!-- dd/mm/yyyy -->
<!ELEMENT primary_sponsor (#PCDATA)>
<!ELEMENT public_title (#PCDATA)>
<!ELEMENT acronym (#PCDATA)>
<!ELEMENT scientific_title (#PCDATA)>
<!ELEMENT scientific_acronym (#PCDATA)>
<!ELEMENT date_enrolment (#PCDATA)><!-- dd/mm/yyyy -->
<!ELEMENT type_enrolment (#PCDATA)>
<!ELEMENT target_size (#PCDATA)>
<!ELEMENT recruitment_status (#PCDATA)><!-- Pending,Recruiting,Suspended,Complete,Other -->
<!ELEMENT url (#PCDATA)>
<!ELEMENT study_type (#PCDATA)><!-- interventional,observational -->
<!ELEMENT study_design (#PCDATA)>
<!ELEMENT phase (#PCDATA)>
<!ELEMENT hc_freetext (#PCDATA)>
<!ELEMENT i_freetext (#PCDATA)>
<!ELEMENT results_actual_enrolment (#PCDATA)>
<!ELEMENT results_date_completed (#PCDATA)><!-- dd/mm/yyyy -->
<!ELEMENT results_url_link (#PCDATA)>
<!ELEMENT results_summary (#PCDATA)>
<!ELEMENT results_date_posted (#PCDATA)><!-- dd/mm/yyyy -->
<!ELEMENT results_date_first_publication (#PCDATA)><!-- dd/mm/yyyy -->
<!ELEMENT results_baseline_char (#PCDATA)>
<!ELEMENT results_participant_flow (#PCDATA)>
<!ELEMENT results_adverse_events (#PCDATA)>
<!ELEMENT results_outcome_measures (#PCDATA)>
<!ELEMENT results_url_protocol (#PCDATA)>
<!ELEMENT results_IPD_plan (#PCDATA)>
<!ELEMENT results_IPD_description (#PCDATA)>


<!ELEMENT contacts (contact+)>
<!ELEMENT contact (type,firstname,middlename,lastname,address,city,country1,zip,telephone,email,affiliation)>
<!ELEMENT type (#PCDATA)><!-- Public,Scientific -->
<!ELEMENT firstname (#PCDATA)>
<!ELEMENT middlename (#PCDATA)>
<!ELEMENT lastname (#PCDATA)>
<!ELEMENT address (#PCDATA)>
<!ELEMENT city (#PCDATA)>
<!ELEMENT country1 (#PCDATA)>
<!ELEMENT zip (#PCDATA)>
<!ELEMENT telephone (#PCDATA)>
<!ELEMENT email (#PCDATA)>
<!ELEMENT affiliation (#PCDATA)>

<!ELEMENT countries (country2+)>
<!ELEMENT country2 (#PCDATA)>

<!ELEMENT criteria (inclusion_criteria,agemin,agemax,gender,exclusion_criteria)>
<!ELEMENT inclusion_criteria (#PCDATA)>
<!ELEMENT agemin (#PCDATA)>
<!ELEMENT agemax (#PCDATA)>
<!ELEMENT gender (#PCDATA)>
<!ELEMENT exclusion_criteria (#PCDATA)>

<!ELEMENT health_condition_code (hc_code+)>
<!ELEMENT hc_code (#PCDATA)>

<!ELEMENT health_condition_keyword (hc_keyword+)>
<!ELEMENT hc_keyword (#PCDATA)>

<!ELEMENT intervention_code (i_code+)>
<!ELEMENT i_code (#PCDATA)>

<!ELEMENT intervention_keyword (i_keyword+)>
<!ELEMENT i_keyword (#PCDATA)>

<!ELEMENT primary_outcome (prim_outcome+)>
<!ELEMENT prim_outcome (#PCDATA)>

<!ELEMENT secondary_outcome (sec_outcome+)>
<!ELEMENT sec_outcome (#PCDATA)>

<!ELEMENT secondary_sponsor (sponsor_name+)>
<!ELEMENT sponsor_name (#PCDATA)>

<!ELEMENT secondary_ids (secondary_id+)>
<!ELEMENT secondary_id (sec_id,issuing_authority)>
<!ELEMENT sec_id (#PCDATA)>
<!ELEMENT issuing_authority (#PCDATA)>

<!ELEMENT source_support (source_name+)>
<!ELEMENT source_name (#PCDATA)>

<!ELEMENT ethics_reviews (ethics_review+)>
<!ELEMENT ethics_review (status,approval_date,contact_name,contact_address,contact_phone,contact_email)>
<!ELEMENT status (#PCDATA)><!-- Not approved,Approved,NA -->
<!ELEMENT approval_date (#PCDATA)><!-- dd/mm/yyyy -->
<!ELEMENT contact_name (#PCDATA)>
<!ELEMENT contact_address (#PCDATA)>
<!ELEMENT contact_phone (#PCDATA)>
<!ELEMENT contact_email (#PCDATA)>
]>
<trials>
  <trial>
    <main>
      <trial_id>IRCT2013012012204N1</trial_id>
      <utrn></utrn>
      <reg_name>IRCT</reg_name>
      <date_registration>2013-12-09</date_registration>
      <primary_sponsor>Vice chancellor for research,  Qazvin University of Medical Sciences</primary_sponsor>
      <public_title>The effect of Intrathecal Atropine to prevent Nausea &amp; Vomiting after surgeries due to use Intrathecal Morphine in lower limb surgeries</public_title>
      <acronym></acronym>
      <scientific_title>The effect of Intrathecal Atropine to prevent Nausea &amp; Vomiting after surgeries due to use Intrathecal Morphine in lower limb surgeries</scientific_title>
      <scientific_acronym></scientific_acronym>
      <date_enrolment>2013-03-05</date_enrolment>
      <type_enrolment>anticipated</type_enrolment>
      <target_size>120</target_size>
      <recruitment_status>Complete</recruitment_status>
      <url>https://irct.ir/trial/12310</url>
      <study_type>interventional</study_type>
      <study_design>Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment.</study_design>
      <phase>2-3</phase>
      <hc_freetext>Spinal Anesthesia.</hc_freetext>
      <i_freetext>Intervention 1: GroupB Spinal Anesthesia was induced using 2.5 cc of 0.5 % Hyperbaric Bupivacaine and 0.2 mg (1cc) of Intrathecal Morphine. In addition patients in group B  received 1cc of saline 0.9%. Intervention 2: Group A Spinal Anesthesia was induced using 2.5 cc of 0.5 % Hyperbaric Bupivacaine and 0.2 mg (1cc) of Intrathecal Morphine.  In addition patients in groupA received 0.1 mg (1cc) Intrathecal Atropine.</i_freetext>
      <results_actual_enrolment></results_actual_enrolment>
      <results_date_completed></results_date_completed>
      <results_url_link></results_url_link>
      <results_summary></results_summary>
      <results_date_posted></results_date_posted>
      <results_date_first_publication></results_date_first_publication>
      <results_baseline_char></results_baseline_char>
      <results_participant_flow></results_participant_flow>
      <results_adverse_events></results_adverse_events>
      <results_outcome_measures></results_outcome_measures>
      <results_url_protocol></results_url_protocol>
      <results_IPD_plan></results_IPD_plan>
      <results_IPD_description></results_IPD_description>
    </main>
    <contacts>
      <contact>
        <type>public</type>
        <firstname>Fatemeh Shima Hadipourzadeh</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Qazvin University of Medical  Sciences,  Navab Street</address>
        <city>Qazvin</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip></zip>
        <telephone>+98 28 1333 6001</telephone>
        <email>fhadipourzade@qums.ac.ir</email>
        <affiliation>Qazvin University of  Medical Sciences</affiliation>
      </contact>
      <contact>
        <type>scientific</type>
        <firstname>Fatemeh Shima Hadipourzadeh</firstname>
        <middlename></middlename>
        <lastname></lastname>
        <address>Qazvin University of  Medical  Sciences,  Navab Street,  Qazvin</address>
        <city>Qazvin</city>
        <country1>Iran (Islamic Republic of)</country1>
        <zip></zip>
        <telephone>+98 28 1333 6001</telephone>
        <email>fhadipourzade@qums.ac.ir</email>
        <affiliation>Qazvin University of Medical Sciences</affiliation>
      </contact>
    </contacts>
    <countries>
      <country2>Iran (Islamic Republic of)</country2>
    </countries>
    <criteria>
      <inclusion_criteria>Participants including major eligibility criteria:&#13;
The  patients aged from 40-70 years  &#13;
      Participants excluding major eligibility criteria:&#13;
Patients with history Neurologic disease and Neuromuscular;  Diabetes Mellitus; Patients with Neuropathy Peripheral;  Infection in site of injection; Sensitivity to Local Anesthesia;  Patients with Vomiting and Nausea before surgery or receiving 48 hours before surgery Anti Vomiting and Nausea;  Women in period of mense</inclusion_criteria>
      <agemin>40 years</agemin>
      <agemax>70 years</agemax>
      <gender>Both</gender>
      <exclusion_criteria></exclusion_criteria>
    </criteria>
    <health_condition_code>
      <hc_code>T41.3</hc_code>
    </health_condition_code>
    <health_condition_keyword>
      <hc_keyword>local anaesthetics</hc_keyword>
    </health_condition_keyword>
    <intervention_code>
      <i_code>Placebo</i_code>
      <i_code>Treatment - Drugs</i_code>
    </intervention_code>
    <intervention_keyword>
      <i_keyword>GroupB Spinal Anesthesia was induced using 2.5 cc of 0.5 % Hyperbaric Bupivacaine and 0.2 mg (1cc) of Intrathecal Morphine. In addition patients in group B  received 1cc of saline 0.9%.</i_keyword>
      <i_keyword>Group A Spinal Anesthesia was induced using 2.5 cc of 0.5 % Hyperbaric Bupivacaine and 0.2 mg (1cc) of Intrathecal Morphine.  In addition patients in groupA received 0.1 mg (1cc) Intrathecal Atropine</i_keyword>
    </intervention_keyword>
    <primary_outcome>
      <prim_outcome>Incidence of  Vomiting and Nausea. Timepoint: Incidence of  Nausea  and  Vomiting  were studied  in patients within 24  hours after injection of Atropine:  Hourly up to 6 hours, Then 6  hours  later and Finally 12  hours later. Method of measurement: With checklist:  Mild;  Moderate;  Severe.</prim_outcome>
    </primary_outcome>
    <secondary_outcome>
      <sec_outcome>Heart  Rate. Timepoint: 3,5,10,15 Minutes after Spinal Anesthesia with receiving Atropin Interathecal. Method of measurement: Heart  Rate per minute.</sec_outcome>
      <sec_outcome>Blood Pressure. Timepoint: 3,5,10,15 Minutes after Spinal Anesthesia with receiving Atropin Intrathecal. Method of measurement: Blood volume pump by heart.</sec_outcome>
      <sec_outcome>With out  pain period. Timepoint: Intrathecal Morphine-Induced Analgesia was studied in 2 hours intervals for 12  hours after injection. Method of measurement: With checklist.</sec_outcome>
    </secondary_outcome>
    <secondary_sponsor>
      <sponsor_name></sponsor_name>
    </secondary_sponsor>
    <secondary_ids>
      <secondary_id>
        <sec_id></sec_id>
        <issuing_authority></issuing_authority>
      </secondary_id>
    </secondary_ids>
    <source_support>
      <source_name>Vice chancellor for research,  Qazvin University of Medical Sciences</source_name>
    </source_support>
    <ethics_reviews>
      <ethics_review>
        <status>Approved</status>
        <approval_date>2013-02-27</approval_date>
        <contact_name>Ethics Comitia Qazvin University of  Medical Sciences</contact_name>
        <contact_address>Qazvin University of Medical Sciences,  Navab Street,  Qazvin Qazvin  Iran (Islamic Republic of)</contact_address>
        <contact_phone></contact_phone>
        <contact_email></contact_email>
      </ethics_review>
    </ethics_reviews>
  </trial>
</trials>
