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Completed Phase 3 Interventional Results available

Phase 3 Study of Efficacy and Safety of the XaraColl® Bupivacaine Implant After Hernioplasty

ClinicalTrials.gov ID: NCT02525133

Public ClinicalTrials.gov record NCT02525133. 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 Jul 22, 2026, 1:43 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 Phase 3, Randomized, Double-blind, Placebo-controlled Study to Investigate the Efficacy and Safety of the XaraColl® Bupivacaine Implant (300 mg Bupivacaine Hydrochloride) After Open Laparotomy Hernioplasty

Study identification

NCT ID
NCT02525133
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Innocoll
Industry
Enrollment
319 participants

Conditions and interventions

Interventions

  • XaraColl Drug
  • Placebo Other

Drug · Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
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
Sep 4, 2015
Primary completion
Apr 21, 2016
Completion
Apr 21, 2016
Last update posted
Jan 7, 2021

2015 – 2016

United States locations

U.S. sites
24
U.S. states
15
U.S. cities
22
Facility City State ZIP Site status
Not listed Anniston Alabama 36207
Not listed Birmingham Alabama 35216
Not listed Anaheim California 92801
Not listed Laguna Hills California 92653
Not listed Pasadena California 91105
Not listed Placentia California 92870
Not listed Aurora Colorado 80045
Not listed Miami Florida 33134
Not listed Miami Florida 33155
Not listed Pembroke Pines Florida 33028
Not listed Pensacola Florida 32503
Not listed Columbus Georgia 31904
Not listed Chicago Illinois 60645
Not listed Las Vegas Nevada 89104
Not listed Durham North Carolina 27710
Not listed Cleveland Ohio 44106
Not listed Columbus Ohio 43210
Not listed Oklahoma City Oklahoma 73104
Not listed Philadelphia Pennsylvania 19104
Not listed Houston Texas 77004
Not listed Houston Texas 77024
Not listed Salt Lake City Utah 84124
Not listed Newport News Virginia 23606
Not listed Madison Wisconsin 53792

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 NCT02525133, 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 Jan 7, 2021 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02525133 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →