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NCT05871762: COMREC

Choice of the Optimal Treatment Strategies for Mid-low REctal Cancer

Recruiting now Last updated 28 August 2023
What this trial tests

trial testing Registry study, no specific intervention in Rectal Neoplasms in 3,705 participants. Currently enrolling.

Timeline
4 June 2023
Primary endpoint
17 May 2027
17 May 2027

Quick facts

Lead sponsorPeking Union Medical College Hospital
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment3,705
Start date4 June 2023
Primary completion17 May 2027
Estimated completion17 May 2027
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Peking Union Medical College Hospital

Who can join

Eligibility, any sex, with Rectal Neoplasms. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to compare the efficacy, prognosis, health economics of different treatment modalities of mid-low rectal cancer in different centers in China, and to conduct cost utility analysis (CUA) on the treatment process of rectal cancer to explore the best treatment modality that meets the actual need of medical units in each region and at each level. The investigators hope to provide evidence-based medical suggestions for medical quality control of rectal cancer and revision of clinical guidelines, and provides a source of decision making for medical management and medical insurance.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Rectal Neoplasms

Currently open trials in the same condition.

Other Peking Union Medical College Hospital trials

Trials by the same sponsor.

Verify against primary sources

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/NCT05871762.

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