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ssTAP vs TAP Catheters in TAH

Comparing the Efficacy of Transversus Abdominis Plane Block, Both Single Injection and Continuous Block Technique, to Wound Infiltration for Total Abdominal Hysterectomy: A Prospective Randomized Study

Status
Terminated
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02525900
Enrollment
15
Registered
2015-08-18
Start date
2016-09-12
Completion date
2018-06-05
Last updated
2018-07-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Pain

Brief summary

Prospective, randomized study comparing local wound infiltration with local anesthetic (LA) versus single injection TAP blocks (ssTAP) with LA versus continuous TAP block (TAP caths) catheters with LA for treatment of postoperative pain after total abdominal hysterectomy (TAH).

Interventions

PROCEDUREWound Infiltration

Wound Infiltration with 0.25% Bupivacine

PROCEDURETAP Blocks

bilateral TAP block with 0.25% Bupivacaine

PROCEDURETAP Catheters

bilateral TAP Catheter with repeat bolus of 0.25% Bupivacaine

Sponsors

University of Arkansas
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Scheduled to undergo total abdominal hysterectomy * Age ≥ 18 years. * American Society of Anesthesiologists (ASA) physical status ≤ 3

Exclusion criteria

* Known coagulopathy * Known allergy to Bupivacaine or morphine * Contraindication to Tylenol usage * Medical conditions contraindicated to bupivacaine use * Daily narcotic usage for ≥ 2 weeks of 20mg of oxycodone daily or an equivalent.

Design outcomes

Primary

MeasureTime frameDescription
Total morphine consumption postoperatively for pain management as measured by the Visual Analog Scale (VAS) pain scale.Up to 48 hours post treatmentThe total morphine consumption used post operatively to manage pain will be measured utilizing the VAS pain scale with 0 being no pain and 10 being as much pain as can be tolerated.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026