Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01848951 · ClinicalTrials.gov registry record

Comparison of Epidural and TAP Block in Abdominal Surgery

A clinical trial of Surgery and Acute Pain, sponsored by University of Nebraska.

Completed
Registry status
72
Enrollment target
1
Study location

NCT01848951: Completed study of Surgery and Acute Pain, sponsored by University of Nebraska.

NCT01848951 is a study of Surgery and Acute Pain that has completed, run by University of Nebraska. The registered enrollment target is 72 participants, below the 52,851-participant average among 120 other Surgery trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01848951, a study of Surgery and Acute Pain, has completed, sponsored by University of Nebraska.

COMPLETED
Registry status
72 participants
Enrollment target
1
Study location

Study Summary

This study will compare the infiltrative transversusabdominis plane (TAP) block with liposomal bupivacaine to epidural analgesia (EA) in major abdominal surgery . The efficacy of the TAP block for abdominal surgery is well documented in literature, but there are no studies utilizing long-acting bupivacaine. The investigators believe the study will demonstrate no difference between the two in terms of pain scores and opioid consumption, but TAP blocks will decreased costs, urinary retention, and hypotension.

Primary Outcome

Comparison of pain scores (0 = no pain to 10 = worst pain possible)

Interventions

  • DRUG Epidural
  • DRUG TAP Block

Study Locations (1)

Nebraska

  • University of Nebraska Medical Center - Omaha

Trial Details

FieldValue
Enrollment Target 72 participants
Start Date 2014-02-01
Est. Completion 2016-12-01
University of Nebraska

407 total trials

What the finished NCT01848951 record still lists

NCT01848951 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 72 participants, a relatively small participant target, below the 52,851-participant average among 120 other Surgery trials with a reported enrollment target (100% lower).

The record links to 3 conditions, with Surgery appearing as the primary indexed condition, and to 2 interventions - of which Epidural is the first listed.

NCT01848951 reports a single indexed study location in Nebraska.

Frequently Asked Questions

What is clinical trial NCT01848951 about?

NCT01848951 is a clinical study titled "Comparison of Epidural and TAP Block in Abdominal Surgery". This study will compare the infiltrative transversusabdominis plane (TAP) block with liposomal bupivacaine to epidural analgesia (EA) in major abdominal surgery . The efficacy of the TAP block for abdominal surgery is well documented in literature, but there are no studies utilizing long-acting bupi...

What is the current status of trial NCT01848951?

This trial is currently completed. The enrollment target is 72 participants. The study started on 2014-02-01. Estimated completion is 2016-12-01.

What conditions does trial NCT01848951 study?

This clinical trial studies the following conditions: Surgery, Acute Pain, Regional Anesthesia.

What interventions are being tested in trial NCT01848951?

The interventions under investigation include: Epidural (DRUG), TAP Block (DRUG).

Who is sponsoring clinical trial NCT01848951?

This trial is sponsored by University of Nebraska, which has 407 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01848951 being conducted?

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

Similar trials for Surgery

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT01848951's enrollment target sits among peer trials

72 75th of 120 higher than 45 of 120 other Surgery trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Surgery trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02359253 · 72 participants · NA

    Robot Aided Rehabilitation - Intervention

  • NCT02962661 · 72 participants · Phase 1

    Donor Bone Marrow Derived Mesenchymal Stem Cells in Controlling Heart Failure in Patients With Cardiomyopathy Caused by Anthracyclines

  • NCT03113643 · 72 participants · Phase 1

    SL-401 in Combination With Azacitidine or Azacitidine/Venetoclax in Acute Myeloid Leukemia (AML), High-Risk Myelodysplastic Syndrome (MDS) or Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN)

  • NCT03187535 · 72 participants · NA

    Effect of TEAS on PONV After Spinal Surgery

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT01848951, the US trial registry maintained by the National Library of Medicine. NCT01848951 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.