Laparoscopic Sentinel Lymph Node Localization in Operable Cervix Cancer

Laparoscopic Sentinel Lymph Node Localization in Patients With Operable Cervical Cancer - A Pilot Study

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00205010

Enrollment

Registered

2005-09-20

Start date

2003-10-31

Completion date

2006-06-30

Last updated

2019-11-19

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

Conditions

Cervical Cancer

Brief summary

The purpose of this study is to evaluate the feasibility, safety and efficacy of laparoscopic ovarian transposition in women less than 40 years of age with locally advanced cervical squamous cell carcinoma

Interventions

PROCEDURELymphoscintigraphy

Study design

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Stage IAI to IIA cervix cancer undergoing primary surgical management

Exclusion criteria

* Previous pelvic dissection * Previous para-aortic lymph node dissection * Evidence of distant mets

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026