Skip to main content
Clinical Trials/NCT02409407
NCT02409407
Unknown
Phase 2

Effectiveness of Oral Versus Vaginal Misoprostol Before Office Hyteroscopy in Infertile Patients

Kasr El Aini Hospital1 site in 1 country120 target enrollmentApril 2015

Overview

Phase
Phase 2
Intervention
Misoprostol , Prostaglandins E1 analogue
Conditions
Infertility
Sponsor
Kasr El Aini Hospital
Enrollment
120
Locations
1
Primary Endpoint
level of pelvic pain according to a 10-point visual analogue scale (VAS)
Last Updated
11 years ago

Overview

Brief Summary

The role of hysteroscopy in infertility investigation is to detect possible intrauterine changes that could interfere with implantation or growth or both of the conceptus, with the invention of miniature hysteroscope, it is possible to perform hysteroscopy in an office setting (Outpatient hysteroscopy; OH), for diagnostic and certain therapeutic intervention. It is currently acknowledged as the 'gold standard' investigation of the intrauterine abnormalities.

Cervical priming prior to diagnostic hysteroscopy softens the cervix and lessens the force needed for dilation, thereby potentially reducing the probability of procedural complication such as uterine perforation, cervical laceration, failure to dilate, and creation of a false track that can occur during cervical entry.

Misoprostol is a prostaglandin El analogue, that can be administered either orally or vaginally, that can cause cervical ripening by inducing collagenolytic activity and synthesis of proteoglycans.

Registry
clinicaltrials.gov
Start Date
April 2015
End Date
May 2016
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Kasr El Aini Hospital
Responsible Party
Principal Investigator
Principal Investigator

Yomna Ali Bayoumi

Lecturer of Obstetrics and Gynecology

Kasr El Aini Hospital

Eligibility Criteria

Inclusion Criteria

  • Female patients aged from 20 to 40 years old.
  • They are complaining with primary or secondary infertility.
  • They undergo investigations including husband semen analysis, hormonal assay, U/S, Hystrosalpingography.

Exclusion Criteria

  • Known sensitivity to misoprostol.
  • Any systemic disease contraindicating the use of prostaglandins (cardiovascular disease, hypertension, renal failure, etc).
  • Concomitant neurologic disease that could affect the correct evaluation of pain.
  • Pregnancy.
  • Any contraindication to hysteroscopy such as Pelvic inflammatory disease (PID).
  • Heavy uterine bleeding.
  • Any uterine abnormality such as pinhole cervix that would obviate passage of a catheter through the cervix.

Arms & Interventions

Oral Misoprostol

oral misoprostol ( prostaglandins E1 analogue) will be administered at a dose of 600 µg (200 µg every 8 hours), starting 24 hours before office hysteroscopy.

Intervention: Misoprostol , Prostaglandins E1 analogue

Vaginal Misoprostol

vaginal misoprostol ( prostaglandins E1 analogue)will be administered at a dose of 400 µg (200 µg 12 hours apart, starting 24 hours before office hysteroscopy)

Intervention: Misoprostol , Prostaglandins E1 analogue

Outcomes

Primary Outcomes

level of pelvic pain according to a 10-point visual analogue scale (VAS)

Time Frame: 10 months

The level of pelvic pain will be rated according to a 10-point visual analogue scale (VAS). The VAS will be applied immediately after the procedure ended

Study Sites (1)

Loading locations...

Similar Trials