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Recruiting Phase 1 NCT06714279

NCT06714279 Laparoscopic-Assisted Transversus Abdominus Plane Block Versus Intraperitoneal Irrigation of Local Anesthetic for Patients Undergoing Laparoscopic Cholecystectomy

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Clinical Trial Summary
NCT ID NCT06714279
Status Recruiting
Phase Phase 1
Sponsor Royal College of Surgeons, Ireland
Condition Laparoscopic Cholecystectomy
Study Type INTERVENTIONAL
Enrollment 144 participants
Start Date 2025-03-12
Primary Completion 2026-06

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Tap Block - BupivacaineIntraperitoneal infiltration to liver

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

Phase 1 is the earliest stage of human testing — safety and dosage are the primary focus. Visits are frequent and medical supervision is intensive. You will be among the first people to receive this treatment.

This trial targets 144 participants in total. It began in 2025-03-12 with a primary completion date of 2026-06.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study is being performed to investigate whether the administration of local anaesthetic into the muscles in the abdomen or onto squirting the local anaesthetic onto the liver following keyhole gallbladder surgery is more beneficial in reducing pain post-operatively. Keyhole gallbladder surgery is typically performed under general anaesthesia (or while the patient is 'fully asleep'), however doctors use other pain relief types to reduce pain after the operation. One of these options is local anaesthetic, which involves the injection of an medication into or onto the part of the body which has been operated on. The reason for doing this is to reduce the pain felt by the patient in the part if the body where the operation occurred. The best way of using these medications remain unclear. The local anaesthetic being used in the study is fully approved for use in Ireland and the drug itself is not being tested. In other words, the drug is not an experimental drug. Local anaesthetic drugs are given in different ways in patients who have just had the keyhole surgery on their gall bladder (this is the surgery that you are about to have). Therefore, the aim of this study is to compare two ways of giving patients these local anaesthetic medications following key-hole gallbladder surgery. These include (1) injecting the medication into the skin at the surgical wounds and squirting it onto the liver (where the gallbladder has been removed from), or (2) injecting the medication into the skin at the surgical wounds and into the muscles in the abdomen (known formally as a transversus abdominus plane block).

Eligibility Criteria

Inclusion Criteria: * Adult patients aged 18 years or older will be considered for recruitment into this study if they are indicated to undergo elective laparoscopic cholecystectomy Exclusion Criteria: * Patients failing to meet the above inclusion criteria.

Contact & Investigator

Central Contact

Matthew G Davey, MB BCh BAO MCh MRCSI PhD

✉ matthewdavey21@rcsi.ie

📞 +353180320000

Principal Investigator

Arnold DK Hill, MB MCh FRCS

PRINCIPAL INVESTIGATOR

RCSI

Frequently Asked Questions

Who can join the NCT06714279 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Laparoscopic Cholecystectomy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT06714279 trial and what does that mean for participants?

Phase 1 trials are the first stage of human testing. The primary goal is to assess safety and determine appropriate dosage levels. Participants are closely monitored. These trials typically involve a small number of volunteers.

Is NCT06714279 currently recruiting?

Yes, NCT06714279 is actively recruiting participants. Contact the research team at matthewdavey21@rcsi.ie for enrollment information.

Where is the NCT06714279 trial being conducted?

This trial is being conducted at Dublin, Ireland.

Who is sponsoring the NCT06714279 clinical trial?

NCT06714279 is sponsored by Royal College of Surgeons, Ireland. The principal investigator is Arnold DK Hill, MB MCh FRCS at RCSI. The trial plans to enroll 144 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology