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Completed Phase 2 Interventional Results available

A Study to Evaluate LB1148 for Return of Gastrointestinal Function and Adhesions in Subjects Undergoing Bowel Resection

ClinicalTrials.gov ID: NCT02836470

Public ClinicalTrials.gov record NCT02836470. 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, 4:46 PM 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 Randomized, Double-Blind, Placebo-Controlled Proof of Concept Study to Evaluate LB1148 for Return of Gastrointestinal Function, Post-Operative Ileus and Intra-Abdominal Adhesions in Subjects Undergoing Elective Bowel Resection

Study identification

NCT ID
NCT02836470
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Palisade Bio
Industry
Enrollment
112 participants

Conditions and interventions

Interventions

  • LB1148 Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 80 Years
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 30, 2019
Primary completion
Sep 5, 2023
Completion
Sep 7, 2023
Last update posted
Jun 20, 2024

2019 – 2023

United States locations

U.S. sites
28
U.S. states
15
U.S. cities
23
Facility City State ZIP Site status
Site 315 Mobile Alabama 36617
Site 307 Yuma Arizona 85364
Site 329 Irvine California 92868
Site 310 Pasadena California 91105
Site 302 Sylmar California 91342
Site 312 Torrance California 90502
Site 306 Clearwater Florida 33756
Site 303 Miami Florida 33125
Site 331 Miami Florida 33126
Site 305 Miami Florida 33142
Site 308 Orlando Florida 32804
Site 328 Louisville Kentucky 40202
Site 321 Baltimore Maryland 21237
Site 324 Burlington Massachusetts 01850
Site 325 Rochester Minnesota 55905
Site 317 New York New York 10029
Site 323 New York New York 10075
Site 318 Chapel Hill North Carolina 27599
Site 301 Cleveland Ohio 44195
Site 322 Pittsburgh Pennsylvania 15212
Site 330 Wynnewood Pennsylvania 19096
Site 327 Charleston South Carolina 29425
Site 320 Dallas Texas 75390
Site 316 Fort Worth Texas 76104
Site 311 Houston Texas 77024
Site 319 Houston Texas 77030
Sie 309 Houston Texas 77089
Site 326 Salt Lake City Utah 84132

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 NCT02836470, 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 Jun 20, 2024 · 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 NCT02836470 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →