Actively Recruiting

Phase Not Applicable
Age: 21Years - 60Years
All Genders
NCT06083298

Multifidus Cervicis and Inter-Semispinal Plane Blocks in Analgesia After Cervical Spine Surgery

Led by Zagazig University · Updated on 2025-07-17

105

Participants Needed

1

Research Sites

127 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Major spine surgery with multilevel instrumentation is followed by a large amount of opioid consumption, significant pain, and difficult mobilization Pain is one of the main factors limiting ambulation, increasing the risk of thromboembolism by immobility, and causing metabolic changes that affect other systems. Therefore, individualized pain management with the use of appropriate analgesic techniques is of paramount importance. Moreover, early intervention in rehabilitation aiming at a better postoperative recovery may reduce the length of hospital stay and return to daily activity. Effective pain management is one of the crucial components in enhanced recovery after surgery (ERAS). Numerous regional anesthetic techniques have been used to provide analgesia following cervical spine surgery, including patient-controlled epidural analgesia, cervical paravertebral block, cervical plexus block, cervical erector spinae plane blocks, and local infiltration analgesia, however, each of these techniques has specific limitations that prevent them from being the analgesic technique of choice for such surgeries. Up to the author's knowledge, there is no study done to compare multifidus cervicis plane block versus inter-semispinal plane block in a randomized controlled clinical trial as preemptive analgesia in patients undergoing cervical spine surgery.

CONDITIONS

Official Title

Multifidus Cervicis and Inter-Semispinal Plane Blocks in Analgesia After Cervical Spine Surgery

Who Can Participate

Age: 21Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient acceptance
  • Age 21 to 60 years old
  • Body mass index (BMI) of 30 kg/m2 or less
  • American Society of Anesthesiologists (ASA) physical status I or II
  • Elective posterior cervical spine surgery under general anesthesia
Not Eligible

You will not qualify if you...

  • Allergy to local anesthetic agents used in the study
  • Skin lesions at the needle insertion site
  • Bleeding disorders
  • Sepsis
  • Liver disease
  • Psychiatric disorders
  • History of chronic pain or current use of analgesics
  • History of cognitive dysfunction or mental illness

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Faculty of medicine, zagazig university

Zagazig, Alsharqia, Egypt, 4115

Actively Recruiting

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Research Team

S

Shereen E Abd Ellatif, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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