Skip to content

Comparison of sexual functions in patients with carcinoma cervix receiving standard versus shorter radiation schedules

A Prospective, Randomized, Parallel-arm study to compare sexual function in Carcinoma Cervix patients receiving Standard versus Hypofractionated Chemoradiation - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/07/114077
Enrollment
90
Registered
2026-07-15
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: C539- Malignant neoplasm of cervix uteri, unspecified

Interventions

Intervention1: Hypofractionated Chemoradiation followed by Brachytherapy: Arm B - will consist of External Beam Radiotherapy (EBRT) to the pelvis at a dose of 37.5Gy/15# 5 days a week over 3 weeks at

Sponsors

All India Institute of Medical Sciences, AIIMS
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age 18 to 65, Biopsy proven Carcinoma Cervix, Clinically and radiologically disease-free 6 months after RT, ECOG PS less than equal to 2, Willing to participate and provide informed consent, Sexually active or willing to resume sexual activity post-treatment, Stage IB3 to IIIC1, The patient should be able to understand and follow instructions.

Exclusion criteria

Exclusion criteria: Prior pelvic surgery or re-irradiation that alters vaginal anatomy significantly, Severe psychiatric illness or cognitive impairment, Pregnancy or lactation, Medical contraindication to sexual activity, Refusal to participate in rehabilitation activities,Gross HDUN

Design outcomes

Primary

MeasureTime frame
Assessment of Sexual function at 6 months post definitive and hypofractionated Radiotherapy by Female Sexual Function Index questionnaire.Timepoint: Sexual function will be assessed at 6 months post-treatment completion.

Secondary

MeasureTime frame
Vaginal toxicity assessment Dosimetric analysis of Vaginal dose Corelation between Vaginal dosimetry and Sexual FunctionTimepoint: 6 months post treatment

Countries

India

Contacts

Public ContactSibika Malla

National Cancer Institute,AIIMS

karunkamboj04@gmail.com9416613389

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 10, 2026