Clinical Trials Directory

Trials / Completed

CompletedNCT00595725

Intra-Operative Lymphatic Mapping in Patients With Invasive Carcinoma of the Cervix or Endometrial Carcinoma

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
151 (actual)
Sponsor
Memorial Sloan Kettering Cancer Center · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

The purpose of this study is to learn if a surgical technique called intraoperative lymphatic mapping can accurately identify the lymph node that is at greatest risk if endometrial or cervical cancer spreads to the lymph nodes. Early cervical cancer is usually treated by removing the cervix, tissue around the cervix, and the upper vagina. If needed, the uterus is also removed. The treatment also includes removing lymph nodes from the pelvis. Endometrial cancer is usually treated by removing the cervix, uterus, fallopian tubes and ovaries. The treatment also includes removing lymph nodes from the pelvis.

Detailed description

Patients with FIGO stage I endometrial cancer or patients with FIGO stage I-IIA invasive cervical cancer and who will be undergoing surgical management to include a lymphadenectomy. ↓ Injection of radioisotope and preoperative lymphoscintigraphy with Tc99m either the day before or on the day of surgery by the Nuclear Medicine Department. ↓ Intraoperative lymphatic mapping with blue dye and gamma probe. ↓ Hysterectomy, Radical hysterectomy and/or radical trachelectomy and pelvic lymphadenectomy.

Conditions

Interventions

TypeNameDescription
OTHERLymphatic MappingIntra-Operative Lymphatic Mapping

Timeline

Start date
2003-02-01
Primary completion
2011-09-01
Completion
2011-09-01
First posted
2008-01-16
Last updated
2011-09-08

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00595725. Inclusion in this directory is not an endorsement.