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NCT02836535 · ClinicalTrials.gov registry record

The Patient-Perspective of Complications After Colon and Rectum Surgery: A Qualitative Analysis

A clinical trial of Colorectal Cancer, sponsored by Memorial Sloan Kettering Cancer Center.

Completed
Registry status
9
Enrollment target
1
Study location

NCT02836535: Completed study of Colorectal Cancer, sponsored by Memorial Sloan Kettering Cancer Center.

NCT02836535 is a study of Colorectal Cancer that has completed, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 9 participants, below the 1,511-participant average among 369 other Colorectal Cancer trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02836535, a study of Colorectal Cancer, has completed, sponsored by Memorial Sloan Kettering Cancer Center.

COMPLETED
Registry status
9 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to understand the patient experience with an adverse event after surgery. An adverse event is an undesirable experience or complication associated with your surgery.

Conditions Studied

Interventions

  • BEHAVIORAL qualitative interviews

Study Locations (1)

New York

  • Memorial Sloan Kettering Cancer Center - New York

Trial Details

FieldValue
Enrollment Target 9 participants
Start Date 2016-07
Est. Completion 2017-06-28

Sponsor

Memorial Sloan Kettering Cancer Center

1,884 total trials

What the Registry Record Tells You About NCT02836535

The ClinicalTrials.gov registry entry for NCT02836535 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 9 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,511-participant average among 369 other Colorectal Cancer trials with a reported enrollment target (99% lower). The listed sponsor is Memorial Sloan Kettering Cancer Center, which has 1,884 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Colorectal Cancer appearing as the primary indexed condition, and to 1 intervention - of which qualitative interviews is the first listed.

NCT02836535 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT02836535 about?

NCT02836535 is a clinical study titled "The Patient-Perspective of Complications After Colon and Rectum Surgery: A Qualitative Analysis". The purpose of this study is to understand the patient experience with an adverse event after surgery. An adverse event is an undesirable experience or complication associated with your surgery.

What is the current status of trial NCT02836535?

This trial is currently completed. The enrollment target is 9 participants. The study started on 2016-07. Estimated completion is 2017-06-28.

What conditions does trial NCT02836535 study?

This clinical trial studies the following conditions: Colorectal Cancer.

What interventions are being tested in trial NCT02836535?

The interventions under investigation include: qualitative interviews (BEHAVIORAL).

Who is sponsoring clinical trial NCT02836535?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02836535 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.