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Dexmedetomidine Versus Fentanyl Added to Levobupivacaine for Transversus Abdominis Plane (TAP) Block

A

Assiut University

Status and phase

Completed
Phase 2
Phase 1

Conditions

Transversus Abdominis Block

Treatments

Drug: Dexmedetomidine Injection [Precedex]
Drug: fentanyl
Drug: Levobupivacaine

Study type

Interventional

Funder types

Other

Identifiers

NCT03778671
17300222

Details and patient eligibility

About

The perioperative management of pain following lower abdominal surgery can pose a challenge to anesthesia providers. Conventional practice has involved the use of opioids as well as neuraxial analgesic techniques. Unfortunately, these therapies are not without potential risks and side effects. These include nausea, vomiting, pruritus, urinary retention, constipation, respiratory depression, and sedation.

Full description

One method used in this multimodal approach is the transversus abdominis plane block. This block, as first described by Rafi. in 2001, provides analgesia to the anterolateral abdominal wall. In 2007, McDonnell et al. further studied this technique in patients undergoing large-bowel resection. He discovered a reduction in postoperative pain and morphine consumption in the first 24 hours postoperatively, resulting in fewer opioid mediated side effects. In this same year, Hebbard et al. described the use of ultrasound guidance to provide real-time imaging of the muscle layers and needle placement to improve transversus abdominis plane block accuracy. In 2008, Hebbard. described the subcostal approach of transversus abdominis plane block, to target the nerves of the upper abdomen. Transversus abdominis plane blocks continue to be studied and developed as an effective method for providing analgesia for numerous types of transverses abdominis plane block duration is limited to effect of administered local anesthetics.The use of an infusion catheter to administer local anesthetics is an option to prolong the block's duration. Recently, adjuvant medications were added to local anesthetics to prolong the effect of transverses abdominis plane block .

Enrollment

90 patients

Sex

All

Ages

65 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ASA physical status II-III,
  • scheduled for uncomplicated elective paraumbilical hernia repair.

Exclusion criteria

  1. Patient refusal to participate in the study
  2. Patients with coagulopathy or under anticoagulation therapy.
  3. Infection near the site of needle insertion.
  4. Body mass index > 40kg/m2
  5. Patients with any neurological or neuromuscular disorder or history of seizures.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

90 participants in 3 patient groups

Group B
Experimental group
Description:
Patients will receive Levobupivacaine 5%
Treatment:
Drug: Levobupivacaine
Group D
Active Comparator group
Description:
Patients will receive Levobupivacaine 5% + 1 µg/kg dexmedetomedine .
Treatment:
Drug: Dexmedetomidine Injection [Precedex]
Group F
Active Comparator group
Description:
Patients will receive Levobupivacaine 5% + 1µg/kg fentanyl
Treatment:
Drug: fentanyl

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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