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NCT03716414

Evaluation of the Efficacy for Sentinel Lymph Node Policy in High-risk Endometrial Carcinoma

Completed Last updated 23 June 2020
What this trial tests

trial testing SLN mapping in Endometrial Adenocarcinoma in 78 participants. Completed in 16 February 2020.

Timeline
1 November 2018
Primary endpoint
16 February 2020
16 February 2020

Quick facts

Lead sponsorFudan University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment78
Start date1 November 2018
Primary completion16 February 2020
Estimated completion16 February 2020
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Fudan University

Who can join

Adults 18 to 100, female only, with Endometrial Adenocarcinoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To evaluate the efficacy of sentinel lymph node biopsy technique in patients with high-risk endometrial carcinoma, which provides the evidence that sentinel lymph node biopsy technique could substitute the systematic Lymph node dissection(LND).

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Endometrial Adenocarcinoma

Currently open trials in the same condition.

Other Fudan University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03716414.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing