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Completed Phase 2 Interventional Results available

Study to Evaluate Analgesic Effect of IV Administration of Kappa Agonist CR845 For Hysterectomy Surgery

ClinicalTrials.gov ID: NCT01361568

Public ClinicalTrials.gov record NCT01361568. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 24, 2026, 2:54 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-Center, Double-Randomized, Double Blind, Placebo Controlled Study to Evaluate the Analgesic Efficacy and Safety of Intravenous CR845 Dosed Preoperatively and Postoperatively in Patients Undergoing a Laparoscopic Hysterectomy

Brief summary

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

The primary purpose of this study is to determine if CR845 is effective in treating the pain associated with a laparoscopic hysterectomy.

Study identification

NCT ID
NCT01361568
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Cara Therapeutics, Inc.
Industry
Enrollment
203 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
21 Years to 65 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
Jul 2011 (Type not available)
Primary completion
Apr 2012 (Actual)
Completion
Apr 2012 (Actual)
Last update posted
May 29, 2014

2011 – 2012

United States locations

U.S. sites
18
U.S. states
11
U.S. cities
17
Facility City State ZIP Site status
Shoals Clinical Research Associates Florence Alabama 35630 —
Horizon Research Group Mobile Alabama 36606 —
Wilmax Mobile Alabama 36608 —
Drug Research and Analysis Corp Montgomery Alabama 36106 —
Shoals Medical Trials, INC Sheffield Alabama 35660 —
Precision Clinical Trials Phoenix Arizona 85032 —
Woodland Healthcare California Clinical Research, Inc Davis California 95616 —
Olive View-UCLA Medical Center Sylmar California 91342 —
Visions Clinical Research Boynton Beach Florida 33472 —
Riverside Clinical Research Edgewater Florida 32132 —
University of Miami, Dept of Miami Florida 33136 —
Cypress Medical Research Wichita Kansas 67226 —
Cooper University Hospital Camden New Jersey 08103 —
Duke University Durham North Carolina 27710 —
Ohio State University Medical, Dept of Anesthesia Columbus Ohio 43210 —
Palmetto Clinical Research, Greenville South Carolina 29615 —
Chattanooga Medical Research Chattanooga Tennessee 37404 —
Texas Health Care, PLLC Fort Worth Texas 76104 —

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 NCT01361568, 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 May 29, 2014 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01361568 live on ClinicalTrials.gov.

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