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NCT02905045 Clinical Trial

Efficacy of Ketoprofen Before Hysterosalpingography

Pain Relief Clinical Trial

Official title:
Effect of Oral Ketoprofen on Hysterosalpingography Pain: A Randomized Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02905045
Other study ID # KETOHSG
Secondary ID
Status Completed
Phase Phase 3
First received September 14, 2016
Last updated November 11, 2017
Start date October 2016
Est. completion date November 2017

Study information
Verified date November 2017
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

hysterosalpingography can cause pain and discomfort in several ways: Use of the tenaculum to grasp the cervix and straighten the uterus for proper insertion; trans-cervical actions including measuring uterine depth, inserting the cannula; and injection of the dye

Recruitment information / eligibility
Status Completed
Enrollment 100
Est. completion date November 2017
Est. primary completion date July 2017
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria:

- any patient came for Hysterosalpingography

Exclusion Criteria:

- any patient has contraindication to Hysterosalpingography

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Ketoprofen

• placebo

Locations
Country Name City State
Egypt Ahmed Abbas Assiut Cairo

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Mean pain score during the procedure 5 minutes
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