Effect of Oral Choline Supplementation on Postoperative Pain

ClinicalTrials.gov ID: NCT00720343

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Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This research will test whether consuming additional choline before gynecological surgery decreases postoperative pain.

Study identification

NCT ID: NCT00720343
Recruitment status: Completed
Study type: Interventional
Phase: Phase 4
Lead sponsor: Columbia University; Other
Enrollment: 60 participants

Conditions and interventions

Conditions

Interventions

Choline Drug
Placebo Drug

Drug

Eligibility (public fields only)

Age range: 18 Years to 60 Years
Sex: Female
Healthy volunteers: Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date: Feb 2009 (Actual)
Primary completion: Jun 2011 (Actual)
Completion: Dec 2012 (Actual)
Last update posted: Jul 9, 2024

2009 – 2012

United States locations

U.S. sites: 1
U.S. states: 1
U.S. cities: 1

Facility	City	State	ZIP	Site status
New York Presbyterian Hospital	New York	New York	10032	—

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows: Public field values for ClinicalTrials.gov record NCT00720343, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do: No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from: Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh: Last update posted Jul 9, 2024 · Synced Nov 15, 2026