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IRCT2015092224128N1 IRCT 2015-12-26 Vice chancellor, Birjand University of Medical Science Morphine effects in in patients with abdominal pain Effects of Morphine analgesia on diagnostic accuracy of abdominal pain 2014-03-21 anticipated 200 Complete https://irct.ir/trial/20433 interventional Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment, Other design features: Using random number table for sampling, patients with an even medical record number were assigned to the study group and those with an odd medical record number were assigned to the control group. 4 Acute abdomen. Intervention 1: Administration of 0.1 mg/kg Morphine Sulfate (Darou Pakhsh, Iran) in the study group. Intervention 2: Administration of normal saline in equal volume of Morphine Sulfate 0.1 mg/kg as a placebo in the control group.
public Mahtab Ghaemi
Ghaffari Boulvard
Birjand Iran (Islamic Republic of) +98 51 3842 4981 ghaemim881@gmail.com Birjand University of Medical Sciences scientific Dr Mohammad Yarani
Birjand, Department of Surgery, Imam Reza Hospital
Birjand Iran (Islamic Republic of) +98 56 3222 2300 mohammadyarani@gmail.com Birjand University of Medical Science Iran (Islamic Republic of) Inclusion criteria: Any patient with acute abdominal pain Exclusion criteria: Patients less than 18 years old; Pregnancy; Patients with the history of abdominal pain more than 3 days; Hypotension (blood pressure less than 90 mmHg); Traumatic patients; Patients with a history of allergy to morphine and its derivatives 18 years 90 years Both R10.1, R10 Pain localized to upper abdomen; Epigastric pain; Pelvic and perineal pain; Pain localized to other parts of lower abdomen; Other and unspecified abdominal pain: Abdominal tenderness NOS, Colic: NOS, infantile Diagnosis Diagnosis Administration of 0.1 mg/kg Morphine Sulfate (Darou Pakhsh, Iran) in the study group Administration of normal saline in equal volume of Morphine Sulfate 0.1 mg/kg as a placebo in the control group Disease diagnosis. Timepoint: Two hours after intervention. Method of measurement: Physical examination. No secondary outcome measure. Timepoint: -. Method of measurement: -. Vice chancellor, Birjand University of Medical Science Approved 2014-08-20 Ethics committee of Birjand University of Medical Sciences Ghaffari Boulvard Birjand Iran (Islamic Republic of)