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NCT01365156 · ClinicalTrials.gov registry record · Phase 3
Extraperitoneal Para-aortic Lymph Node Dissection (EPLND) for Cervix
A Phase 3 study of Cervical Cancer and Adenocarcinoma, sponsored by M.D. Anderson Cancer Center.
- Completed
- Registry status
- Phase 3
- Development phase
- 28
- Enrollment target
- 3
- Study locations
NCT01365156: Completed Phase 3 study of Cervical Cancer and Adenocarcinoma, sponsored by M.D. Anderson Cancer Center.
NCT01365156 is a Phase 3 study of Cervical Cancer and Adenocarcinoma that has completed, run by M.D. Anderson Cancer Center. The registered enrollment target is 28 participants, below the 570-participant average among 144 other Cervical Cancer trials with a reported enrollment target (95% lower). The trial reports 3 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01365156, a Phase 3 study of Cervical Cancer and Adenocarcinoma, has completed, sponsored by M.D. Anderson Cancer Center.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 28 participants
- Enrollment target
- 3
- Study locations
Study Summary
The goal of this clinical research study is to learn if a surgical procedure called an extraperitoneal laparoscopic lymphadenectomy followed by chemotherapy and tailored radiation therapy can help to control the disease for a longer time than standard-of-care chemotherapy and whole pelvic radiation therapy.
Primary Outcome
To determine if patients with locally advanced cervical cancer have longer overall survivals with pretherapeutic paraaortic surgical staging followed by tailored chemoradiation when compared to patients who undergo standard radiologic staging followed by whole pelvic chemoradiation therapy.
Conditions Studied
Interventions
- RADIATION Chemoradiation
- PROCEDURE Extraperitoneal laparoscopic lymphadenectomy (EPLND)
Study Locations (3)
Texas
- Lyndon B. Johnson General Hospital - Houston
- University of Texas MD Anderson Cancer Center - Houston
Other
- Vall d'Hebron Hospital - Brussels
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 28 participants |
| Start Date | 2011-08 |
| Est. Completion | 2020-01-24 |
| Phase | Phase 3 |
What the finished NCT01365156 record still lists
NCT01365156 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 28 participants, a relatively small participant target, below the 570-participant average among 144 other Cervical Cancer trials with a reported enrollment target (95% lower).
The record links to 5 conditions, with Cervical Cancer appearing as the primary indexed condition, and to 2 interventions - of which Chemoradiation is the first listed.
NCT01365156 reports a single indexed study location in Texas, Other.
Frequently Asked Questions
What is clinical trial NCT01365156 about?
NCT01365156 is a clinical study titled "Extraperitoneal Para-aortic Lymph Node Dissection (EPLND) for Cervix". The goal of this clinical research study is to learn if a surgical procedure called an extraperitoneal laparoscopic lymphadenectomy followed by chemotherapy and tailored radiation therapy can help to control the disease for a longer time than standard-of-care chemotherapy and whole pelvic radiation ...
What is the current status of trial NCT01365156?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 28 participants. The study started on 2011-08. Estimated completion is 2020-01-24.
What conditions does trial NCT01365156 study?
This clinical trial studies the following conditions: Cervical Cancer, Adenocarcinoma, Cervical Squamous Cell Carcinoma, Locally Advanced Malignant Neoplasm, Adenosquamous Carcinoma.
What interventions are being tested in trial NCT01365156?
The interventions under investigation include: Chemoradiation (RADIATION), Extraperitoneal laparoscopic lymphadenectomy (EPLND) (PROCEDURE).
Who is sponsoring clinical trial NCT01365156?
This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01365156 being conducted?
This trial has 3 study locations across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Cervical Cancer
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT01365156's enrollment target sits among peer trials
28 125th of 144 higher than 20 of 144 other Cervical Cancer trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Cervical Cancer trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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