Status:
COMPLETED
Comparison Between the Intrauterine Lidocaine and Warm Saline Distention Medium for Pain Relief During Office Hysteroscopy
Lead Sponsor:
Cairo University
Conditions:
Hysteroscopy
Eligibility:
FEMALE
18-60 years
Phase:
NA
Brief Summary
Procedure: The procedure was done in the lithotomy position during the postmenstrual period. We used a 30° angle 2.9 mm rigid hysteroscopy with 3.8 mm diagnostic sheath \[TEKNO®, LIGHT XA 180, Germa...
Detailed Description
A written consent was taken from eligible women on admission after explaining the aim of the research, procedure, expected value, outcome, and possible adverse effects, with full details provided to t...
Eligibility Criteria
Inclusion
- Age ≥ 18 years old.
- Indications of diagnostic office hysteroscopy as:
- Suspicion of the intracavitary lesion. Abnormal uterine bleeding. Abnormal endometrial thickening. Postmenopausal bleeding. Mullerian congenital anomaly. Removal of foreign bodies. Undergoing the procedure to assess the endocervical canal, uterine cavity, and tubal ostia for infertility.
Exclusion
- Patients with contra-indications of diagnostic hysteroscopy as:
- Unable to exclude pregnancy Acute pelvic infection Active genital herpes Profuse bleeding at the time of the procedure. Any usage of analgesic agent on the day of the procedure. Failure of entry of the cervical canal requiring cervical dilatation. Any additional procedure during the procedure: polypectomy, biopsy and adhesiolysis.
- Patient refusal to participate in the study.
Key Trial Info
Start Date :
September 30 2024
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 12 2025
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT06946121
Start Date
September 30 2024
End Date
April 12 2025
Last Update
April 27 2025
Active Locations (1)
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1
Kasr Alainy medical school
Cairo, Egypt, 12111