Trials / Completed
CompletedNCT04500470
Ketoprofen With or Without Vaginal Isonicotinic Acid Hydrazide Prior to Hysterosalpingography
Ketoprofen With or Without Vaginal Isonicotinic Acid Hydrazide (INH) Prior to Hysterosalpingography in Primarily Infertile Patients: a Randomized Controlled Trial
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 200 (actual)
- Sponsor
- Aswan University Hospital · Academic / Other
- Sex
- Female
- Age
- 18 Years – 40 Years
- Healthy volunteers
- Not accepted
Summary
The aim of our study is to determine the efficacy of Ketoprofen with or without vaginal isonicotinic acid hydrazide on the pain scores during HSG.
Detailed description
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
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ketoprofen + INH | patients will have of oral Ketoprofen 60 minutes before the procedure plus 3 table 900 mg vaginal isonicotinic acid hydrazide by the patient 12 hours before the procedure |
| DRUG | Ketoprofen + placebo | patients will have of oral Ketoprofen 60 minutes before the procedure plus 3 table placebo by the patient 12 hours before the procedure |
Timeline
- Start date
- 2020-09-01
- Primary completion
- 2021-07-30
- Completion
- 2021-09-01
- First posted
- 2020-08-05
- Last updated
- 2022-01-19
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT04500470. Inclusion in this directory is not an endorsement.