Efficacy of Ketoprofen Before Hysterosalpingography

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

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Key information

Conditions

Pain Relief

Age range

20 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 3

Primary location

Ahmed Abbas

Assiut, Cairo Governorate, 002, Egypt

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

any patient came for Hysterosalpingography

Exclusion criteria

any patient has contraindication to Hysterosalpingography

Treatment and study plan

Ketoprofen

Drug

Other names: bi profenid

Placebo

Drug

Primary outcomes

Mean pain score during the procedure

Time frame: 5 minutes

Sponsors and collaborators

Lead sponsor

Assiut University

Other

Registry information

Official study title

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

Important dates

Study start: 2016
Primary completion: 2017
Study completion: 2017
First posted: Sep 19, 2016
Registry last updated: Nov 14, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed