Clinical Trials Directory

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UnknownNCT04500496

Vaginal Dinoprostone Versus Isonicotinic Acid Hydrazide Prior to Diagnostic Office Hysteroscopy

Vaginal Dinoprostone Versus Vaginal Isonicotinic Acid Hydrazide Prior to Diagnostic Office Hysteroscopy in Postmenopausal Patients: a Randomized Controlled Trial

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
Aswan University Hospital · Academic / Other
Sex
Female
Age
45 Years – 60 Years
Healthy volunteers
Not accepted

Summary

To compare the effectiveness of vaginal dinoprostone and vaginal Isonicotinic acid hydrazide in minimizing the pain experienced by postmenopausal patients during diagnostic office hysteroscopy and to assess the ease of insertion of hysteroscope as reported by the hysteroscopist.

Detailed description

hysteroscopy is commonly used in the diagnosis and treatment of intrauterine lesions such as polyps, fibroids, septa, and adhesions, and in the presence of abnormal bleeding and during the removal of an intrauterine device or foreign body. Cervical ripening is made possible by the use of medication through different routes.

Conditions

Interventions

TypeNameDescription
DRUGINH3 tablet of INH inserted by the patient 12 hours before the scheduled office hysteroscopy
DRUGdinoprostone1 vaginal tablet of dinoprostone (3mg) (prostin® E2, Pharmacia \& Upjohn, Puurs, Belgium) inserted by the patient 12 hours before the scheduled office hysteroscopy.

Timeline

Start date
2020-09-01
Primary completion
2021-12-30
Completion
2022-01-30
First posted
2020-08-05
Last updated
2021-09-29

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04500496. Inclusion in this directory is not an endorsement.