Effectiveness and Safety of Percutaneous Adhesiolysis Using Rac'z Catheter Versus Navi Catheter in Management of Failed Back Surgery Syndrome

Sponsor
Assiut University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05018377
Collaborator
(none)
20
1
2
13
1.5

Study Details

Study Description

Brief Summary

In the past decade, spine surgery rates have dramatically increased in parallel to those of other procedural interventions. Persistent pain is a common occurrence after spine surgery, with the most commonly quoted prevalence rates ranging from 10% to 40%. This pain can be classified into failure to alleviate baseline pain, pain resulting from complications (e.g., arachnoiditis and epidural adhesions), and pain that ensues several years later as a sequele to alterations in spinal architecture and biomechanics (e.g., adjacent segment discogenic or facetogenic pain) which is called failed back surgery syndrome ( FBSS )

Condition or Disease Intervention/Treatment Phase
  • Procedure: Racz adhesolysis
  • Device: NAVI adhesolysis
N/A

Detailed Description

By observing adhesions directly, the lysis of scar tissue can be carried out mechanically using some percutaneous techniques as insertion of catheters as Rac'z catheter (thin in calibre) which will be inserted through the skin under fluoroscopy guidance or using NAVI catheter (large in calibre) either fluoroscopy guided or using thin epiduroscopy. Adhesions can be disintegrated and their evaluation scores may improve.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Effectiveness and Safety of Percutaneous Adhesiolysis Using Rac'z Catheter Versus Navi Catheter in Management of Failed Back Surgery Syndrome
Actual Study Start Date :
May 1, 2021
Anticipated Primary Completion Date :
Jun 1, 2022
Anticipated Study Completion Date :
Jun 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Raj'z catheter

Procedure: Racz adhesolysis
adhesiolysis in failed back surgery

Active Comparator: NAVI catheter

Device: NAVI adhesolysis
adhesiolysis in failed back surgery

Outcome Measures

Primary Outcome Measures

  1. Visual analogue scale [6 months]

    The VAS score was used that has 0-10 points. The 0 point represents the painless state and a score from 1 to 3 points represents mild pain, from 4 to 6 points represents moderate pain and from 7 to 10 points represents severe pain.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients with history of lumbar surgery of at least 6 months duration in the past.

  • Patients over the 18 years of age.

  • History of persistent function-limiting lower extremity pain aggravated by "dural tug" (observed when the patient, sitting on the exam table with legs stretched out, bends forward, bringing on the back pain) with or without low back pain of at least 6 months duration after failure of conventional conservative management in most patients including NSAIDS, muscle relaxants (tizanidine, magnesium sulphate) and pregabalin.

  • Patients who are competent to understand the study protocol and provide voluntary, written informed consent and participate in outcome measurements.

Exclusion Criteria:
  • Unstable or heavy opioid use.

  • Uncontrolled psychiatric disorders.

  • Uncontrolled medical illness.

  • Any conditions that could interfere with the interpretation of the outcome assessments.

  • Pregnant or lactating women.

  • Patients with a history or potential for adverse reaction(s) to local anaesthetics or steroid.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Saeid Metwaly Elsawy Assiut Egypt 71111

Sponsors and Collaborators

  • Assiut University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Saeid Metwaly Abouelyazid Elsawy, lecturer of anesthesia, Assiut University
ClinicalTrials.gov Identifier:
NCT05018377
Other Study ID Numbers:
  • saeid
First Posted:
Aug 24, 2021
Last Update Posted:
Aug 24, 2021
Last Verified:
Aug 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Product Manufactured in and Exported from the U.S.:
Yes
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 24, 2021