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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04125771
Other study ID # Diclofenac potassium
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 16, 2020
Est. completion date October 1, 2020

Study information

Verified date October 2021
Source Aljazeera Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Diclofenac is a proven, commonly prescribed nonsteroidal anti-inflammatory drug (NSAID) that has analgesic, anti-inflammatory, and antipyretic properties, and has been shown to be effective in treating a variety of acute and chronic pain and inflammatory conditions.


Description:

Diclofenac is a proven, commonly prescribed nonsteroidal anti-inflammatory drug (NSAID) that has analgesic, anti-inflammatory, and antipyretic properties, and has been shown to be effective in treating a variety of acute and chronic pain and inflammatory conditions. . As with all NSAIDs, diclofenac exerts its action via inhibition of prostaglandin synthesis by inhibiting cyclooxygenase-1 (COX-1)


Recruitment information / eligibility

Status Completed
Enrollment 64
Est. completion date October 1, 2020
Est. primary completion date August 25, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria: - 1. Patients indicated for diagnostic hysteroscopy including infertility, bleeding, suspected intrauterine pathologies (eg polypi , septea) 2. Reproductive age 20 - 40yrs Exclusion Criteria: - 1. Menopausal and amenorrhic patients 2. Contraindication to office hysteroscopy such as:- pelvic inflammatory disease, marked cervical stenosis, pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Diclofenac + HBB with hysteroscopy
Giving Diclofenac + HBB with hysteroscopy
Diclofenav + placebo
Giving Diclofenac + placebo with hysteroscopy

Locations

Country Name City State
Egypt Algazeerah and Kasralainy hospital Giza

Sponsors (2)

Lead Sponsor Collaborator
Aljazeera Hospital Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary The number of women who will not feel pain the effect of medications on pain sensation within half an hour
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