Assessment of quality of cervical tissue taken from two different tools through colposcopy

Phase 3

• Conditions: Health Condition 1: R876- Abnormal cytological findings in specimens from female genital organs

• Registration Number: CTRI/2023/12/060651
• Lead Sponsor: JAWAHARLAL INSTITUTE OF POSTGRADUATE MEDICAL EDUCATION AND RESEARCH

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 January 2024

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

Women aged more than 18 years referred to colposcopy clinic with abnormal pap smear report or HPV DNA positivity or VIA/VILI positive who need colposcopic directed cerrvical biopsy

Exclusion Criteria

Cancer cervix

H/o Total hysterectomy

H/o Radiation exposure

Pelvic inflammatory disease

Pregnancy

Cardiac pacemaker

Requiring multiple biopsies

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To compare the quality of tissue in colposcopy directed cervical biopsy between punch biopsy forceps & round loop electrodeTimepoint: primary outcome will be assessed at 3 weeks and secondary outcome will be assessed at the end of procedure.

Secondary Outcome Measures

Name	Time	Method
To complete the pain between two tools in a colposcopy directed cervical biopsyTimepoint: secondary outcome will be assessed at the end of procedure