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Trials / Unknown

UnknownNCT03675802

Cervical Preparation in Hysteroscopy

Randomized Comparison of Vaginal Dinoprostone and Misoprostol for Cervical Ripening Before Diagnostic Hysteroscopy in Patients Who Have Undergone Cesarean Section

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Aljazeera Hospital · Academic / Other
Sex
Female
Age
20 Years – 42 Years
Healthy volunteers
Accepted

Summary

The hysteroscopy was performed in the proliferativephase of the menstrual cycle. The patients were given generalintravenous anesthesia (propofol/fentanyl) after the vulvar and the vaginal area had been disinfected with a 7.5% Betadinesolution by the surgical nurse All operations were performed by the same surgeon to avoid possible discrepancies between different surgeons.

Detailed description

Astandard rigid30 hysteroscope (Karl Storz bettocchi hysteroscope) with a 30° viewing angleand an outer sheath diameter 5.5 mm, inner sheath diameter 4.3 mm and scope diameter 2.9 mmwas used in all procedures. A speculum was introduced into the vagina, and the uterine cervixwas visualized. Initially, the surgeon attempted to passthrough the cervical canal with the tool directly. When thatwas not possible or when the cervical canal was too rigid ortoo tight, the cervix was grasped with a tenaculum.

Conditions

Interventions

TypeNameDescription
DRUGmisoprostolgiving misoprostol to this group
DRUGdinoprostonegiving dinoprostine

Timeline

Start date
2018-09-23
Primary completion
2019-03-01
Completion
2019-03-15
First posted
2018-09-18
Last updated
2019-01-09

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT03675802. Inclusion in this directory is not an endorsement.

Cervical Preparation in Hysteroscopy (NCT03675802) · Clinical Trials Directory