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RecruitingNCT06633068Updated Oct 9, 2024

The Analgesic Efficacy of Perineural Nalbuphine as an Adjuvant to Bupivacaine in Ultrasound Guided Superficial Cervical Plexus Nerve Block for Thyroid Surgeries. A Double Blinded Randomized Controlled Trial.

A Phase 2 interventional study of Adding perineural Nalbuphine to Bupivacaine in superficial cervical nerve block in Intra and Postoperative Pain Management, sponsored by Cairo University. Recruiting at 1 site in Egypt. Open to participants aged 18 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-10-09.

Sponsored by Cairo University · Phase 2, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Apr 2025, 1 year 6 months ago, but the record still lists the study as recruiting.
  • Started Jul 2024; still recruiting 2 years 2 months later.
Phase
Phase 2
Study type
Interventional
Enrollment
54
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
All
01

Study summary

This study aiming to evaluate the analgesic effect of adding nalbuphine as an adjuvant to bupivacaine in superficial cervical plexus block during thyroid surgeries regarding first rescue analgesia in the first twenty-four hours postoperative, VAS score after extubation and complications such as postoperative nausea, vomiting and respiratory depression.

Read the detailed description

Thyroidectomy is a common and painful procedure demanding analgesia. Patients may experience discomfort in swallowing, burning sensation in the throat, nausea, and vomiting, which are all caused by the surgical procedures or general anaesthesia. Thyroid surgeries induce brief postoperative pain caused by several mechanisms. One of the mechinsims of this Post-operative pain, believed to be due to the interruption of the rich nerve supply present in the neck.

A lot of drugs have been used to decrease this postoperative pain such as non-steroidal anti inflammatory drugs , opioids or regional blocks. Traditionally, opioids have been the mainstay of postoperative analgesia, specifically at thyroid and parathyroid surgical centers, where narcotic analgesics make up the major component of their postoperative pain control regimens. However, the use of opioids has been linked to an increased risk of postoperative complications that include ventilatory depression, sedation, postoperative nausea and vomiting (PONV), pruritis, difficulty of voiding, ileus and surgical site infections which can in turn contribute to delayed hospital discharge. Further acute and chronic opioids can have significant effects on the endocrine system. Longer-term use of opioids may lead to dependence and substance abuse disorder.

The skin overlying the neck, ear, angle of the mandible, shoulder, and clavicle is supplied by the superficial cervical plexus (SCP), which is a sensory neural plexus formed from the ventral rami of the first four cervical nerves (C1-C4). It emerges behind the posterior border of sternomastoid muscle.

Bilateral superficial cervical plexus block (SCPB) has shown good intraoperative and postoperative analgesia in upper neck surgeries especially in thyroidectomies, this regional block can be facilitated by using ultrasound guided technique as it provides good visualisation of the anatomical structures and decreases the complications.

There has always been a search for ideal adjuvants in peripheral nerve blocks which prolong the duration of analgesia with lesser adverse effects, Recently, nalbuphine was studied frequently as an adjuvant to local anesthetics in spinal and epidural and the results of all studies concluded that nalbuphine is effective when used as an adjuvant to local anaesthetics in spinal and epidural as it significantly prolongs the block duration.

The mechanism of perineural nalbuphine has not been clearly identified till now, previous studies demonstrated underlying mechanism could be interpreted that inflammatory response increases the synthesis of opioid receptors in the dorsal root ganglion neurons and enhances axonal transport and accumulation of opioid receptors in the sensory nerve endings in the inflamed tissue. Moreover, nalbuphine is an opioid receptors antagonist that allows for the peripheral analgesic effects of opioids in addition to the analgesic effect of its systemic absorption.

However, nalbuphine has not been studied extensively as an additive for peripheral nerve blocks as there was a minor research about it as an adjuvant to bupivacaine in brachial plexus block for upper limb surgeries and it showed that it prolongs the duration of sensory and motor blockades and reduces the requirement of analgesics in postoperative period. The superficial cervical block is a sensory block carrying sensory nerve fibers only with different axonal chemistry .

To our knowledge, no study till date compared the analgesic effect of perineural nalbuphine as an adjuvant to the superficial cervical block.

02

Conditions studied

  • Intra and Postoperative Pain Management

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03

In context

Pain, Postoperative

5,093 studies on the registry are indexed under Pain, Postoperative; 1,140 are open to participants now.

This study's planned enrollment of 54 is below the median of 75 across 4,344 interventional studies indexed under Pain, Postoperative.

Browse Pain, Postoperative studies →

Lead sponsor

Cairo University is the lead sponsor of 4,780 studies on the registry; 1,427 are open to participants now.

Of its 36 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Patients aged between 18 to 60 years old of both sexes undergoing elective thyroid surgery.
  • ASA I and II.

Exclusion criteria

Exclusion Criteria:

  • Patient refusal.
  • Hypersensitivity or contraindication to nalbuphine or bupivacaine.
  • Pregnancy or lactating mothers.
  • Hepatic, cardiac or renal diseases.
  • Bleeding disorders.
  • Severe neurological or psychological disorders.
  • Goitres with retrosternal extension.
  • Any anatomical disruption in the neck (ex: metastatic lymph nodes).
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Care provider, Investigator)
Enrollment
54 participants (estimated)

Study arms

  • Placebo comparator
    Group (C) control group

    Patients will receive bilateral superficial cervical plexus block with 28 ml bupivacine 0.25% mixed with 2 ml saline 0.9%, to a volume of 30 ml, 15 ml on each side of the neck before induction of general anaesthesia.

    Drug: Adding perineural Nalbuphine to Bupivacaine in superficial cervical nerve block

  • Active comparator
    Group (N) Perineural Nalbuphine

    Patients will receive bilateral superficial cervical plexus block with 28 ml Bupivacaine 0.25% mixed with 10 mg nalbuphine in saline 0.9% to a volume of 30 ml, 15 ml on each side of the neck before induction of general anaesthesia.

    Drug: Adding perineural Nalbuphine to Bupivacaine in superficial cervical nerve block

Interventions

  • DrugAdding perineural Nalbuphine to Bupivacaine in superficial cervical nerve block

    Adding nalbuphine as an adjuvant to bupivacaine in superficial cervical plexus block during thyroid surgeries

06

What researchers measure

Primary outcomes

  1. time to first rescue analgesia (will be given to VAS score > 4) following surgery in the first 24 hours.

    defined as the time interval between the end of surgery and the first request to postoperative Nalbuphine

    Time frame: First 24 hours postoperative

Secondary outcomes

  1. Intraoperative hemodynamics

    mean arterial blood pressure

    Time frame: every 10 minutes until the end of the surgery

  2. VAS score after extubation

    Visual Analogue Scale (VAS) measures pain intensity.

    Time frame: at 0,2,6,12,18 and 24 hours after completion of surgery.

  3. Total amount of nalbuphine administrated to the patient 24 hours postoperative.

    As analgesia

    Time frame: Every one hour postoperative for 24 hours

07

Study locations

1 of 1 sites recruiting
  • Kasr Alainy Teaching Hospitals
    Giza, الجيزة 1111, Egypt
    • Omnia Y Kamel, MD · Contact · omniayehiakamel90@gmail.com · 01270130326
    • Sara M Badie, Master · Sub investigator
    • Nashwa Nabil, Professor · Principal investigator
    • Marwa M Zayed, Ass professor · Sub investigator
    • Amany Eissa, Doctorate · Sub investigator
    • Omnia Y Kamel, Doctorate · Sub investigator
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 9, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06633068
Lead sponsor
Cairo University
Responsible party
Omnia Yahia El Sayed Kamel (Lecturer of anesthesiology and surgical ICU and pain management, Cairo University) — Principal investigator
First posted
Oct 9, 2024
Start date
Jul 15, 2024
Primary completion
Apr 2025 (estimated)
Completion
Jul 2025 (estimated)
Last update
Oct 9, 2024

Study contacts

Sara M Badie, Master degree
Contact
sarabadie1993@gmail.com
0109588821
Nashwa Nabil, Professor
Contact
nashwanabeel@yahoo.com
01001111968
Marwa M Zayed, Assistant professor
study director · Cairo University
Amany Eissa, Doctorate
study director · Cairo University
Omnia Y Kamel, Doctorate degree
study director · Cairo University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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