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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00477061
Other study ID # AG11
Secondary ID
Status Completed
Phase Phase 4
First received May 20, 2007
Last updated May 20, 2007
Start date January 2004
Est. completion date March 2005

Study information

Verified date May 2007
Source Tehran University of Medical Sciences
Contact n/a
Is FDA regulated No
Health authority Iran: Ministry of Health
Study type Interventional

Clinical Trial Summary

The purpose of the study is to evaluate morphine effect on pain reduction and diagnostic accuracy in patients admitted to emergency ward with the diagnosis of acute appendicitis.


Description:

Analgesic administration for pain control in patients with acute abdominal pain, regarding acute appendicitis, is controversial. Despite the results previous studies indicating the safeness of analgesic use in ED for acute abdominal pain, physicians still prefer to postpone their use after performing surgical evaluations. Since many patients admitted to ED are unlikely to receive prompt surgical consultation, many of them need pain relief to prevent unnecessary suffering. On the other hand such pain relief must not interfere with the diagnosis and treatment of patients and do not cause any complications. Morphine is a common and effective analgesic which, if shown to have no effect on correct diagnosis of acute abdomen, can be used for this purpose.

Thus we evaluated morphine effect on pain reduction and diagnostic accuracy in patients admitted to ED with the diagnosis of acute appendicitis.


Recruitment information / eligibility

Status Completed
Enrollment 71
Est. completion date March 2005
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 13 Years to 75 Years
Eligibility Inclusion Criteria:

- clinical signs of acute appendicitis

- planned for appendectomy

- supposed to wait for at least 1 hour in the ED before operation

Exclusion Criteria:

- suspicion to perforated appendicitis

- being under the age of 13

- pregnancy (according to history and ß-HCG result)

- opium addiction

- systolic blood pressure of less than 90 mmHG

- known cases of chronic obstructive pulmonary disease (COPD)

- known sensitivity to morphine

- history of sickle cell disease

- self administration of analgesics before enrollment

- refusal to participate

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

Drug:
Morphine


Locations

Country Name City State
Iran, Islamic Republic of Sina General Hospital Tehran

Sponsors (1)

Lead Sponsor Collaborator
Tehran University of Medical Sciences

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain Intensity
Secondary Diagnostic Accuracy
See also
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