Clinical Trials Directory

Trials / Completed

CompletedNCT04500509

Diclofenac Potassium With or Without Vaginal Dinoprostone Prior to Hysterosalpingography

Diclofenac Potassium With or Without Vaginal Dinoprostone 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 – 45 Years
Healthy volunteers
Not accepted

Summary

The aim of our study is to determine the efficacy of oral diclofenac potassium with or without vaginal dinoprostone prior to hysterosalpingography in primarily infertile patients on the pain scores during HSG.

Detailed description

hysterosalpingography is a diagnosis procedure in the evaluation of infertile women and considered to be the traditional and the gold standard in the assessment of the patency of the fallopian tubes. The major disadvantage of hysterosalpingography is pain. In a study reported the patients complained of moderate to severe pain during the procedure. It is reported that some patients undergoing hysterosalpingography was more stressful and anxiety and effect on pain scores.

Conditions

Interventions

TypeNameDescription
DRUGdiclofenac potassium + dinoprostonepatients will have of oral diclofenac potassium 60 minutes before the procedure plus one tablets of vaginal dinoprostone (6 mg) 6 hours prior to the procedure by the patient
DRUGdiclofenac potassium + placebopatients will have of oral diclofenac potassium 60 minutes before the procedure plus one tablets of vaginal placebo 6 hours prior to the procedure by the patient

Timeline

Start date
2020-09-01
Primary completion
2021-08-01
Completion
2021-10-30
First posted
2020-08-05
Last updated
2022-01-19

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04500509. Inclusion in this directory is not an endorsement.