NCT07853170

Brief Summary

This study aims to compare the 3-needle and 5-needle of genicular nerve block on pain and quality of life in Knee osteoarthritis (KOA).

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
11mo left

Started Oct 2026

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 27, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

October 1, 2026

Completed
14 days until next milestone

Study Start

First participant enrolled

October 15, 2026

Expected
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2027

Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2027

Last Updated

October 1, 2026

Status Verified

September 1, 2026

Enrollment Period

11 months

First QC Date

September 27, 2026

Last Update Submit

September 27, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Degree of pain

    Each patient will be instructed about postoperative pain assessment with the numeric rating scale (NRS) score. NRS (0 represents "no pain" while 10 represents "the worst pain imaginable").

    6 months postoperatively

Secondary Outcomes (3)

  • Measurement of Quality of life

    6 months postoperatively

  • Patients' opioid medication use

    6 months after treatment

  • Degree of patient satisfaction

    6 months postoperatively

Study Arms (2)

Group I (3-nerve-targeted group)

EXPERIMENTAL

Patients will receive 3-nerve protocol.

Other: 3-nerve-targeted group

Group II (5-nerve-targeted group)

EXPERIMENTAL

Patients will receive 5-nerve protocol.

Other: 5-nerve-targeted group

Interventions

Patients will receive 3-nerve protocol.

Group I (3-nerve-targeted group)

Patients will receive 5-nerve protocol.

Group II (5-nerve-targeted group)

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Age ≥18 years.
  • Both sexes.
  • Patients with unilateral chronic knee pain for more than 3 months.
  • Patients received conservative treatment for at least 3 months.
  • Diagnosed Knee osteoarthritis (KOA) according to the American College of Rheumatology (ACR) criteria, and grade greater than or equal to Kellgren-Lawrence grade 2.

You may not qualify if:

  • Chronic knee pain is due to causes other than KOA, such as connective tissue diseases, lumbar radicular neuropathy (spondylolisthesis, spinal stenosis), or sciatic pain.
  • Knee effusion.
  • Neuro/psychiatric disorders.
  • History of intra-articular injection in the prior 3 months.
  • Prior knee surgery.
  • Active systemic or local knee infections; anticoagulant use.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Tanta University

Tanta, El-Gharbia, 31527, Egypt

Location

Related Publications (1)

  • Geng R, Li J, Yu C, Zhang C, Chen F, Chen J, Ni H, Wang J, Kang K, Wei Z, Xu Y, Jin T. Knee osteoarthritis: Current status and research progress in treatment (Review). Exp Ther Med. 2023 Aug 25;26(4):481. doi: 10.3892/etm.2023.12180. eCollection 2023 Oct.

MeSH Terms

Conditions

PainOsteoarthritis, Knee

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsOsteoarthritisArthritisJoint DiseasesMusculoskeletal DiseasesRheumatic Diseases

Central Study Contacts

Mohammed S Elsharkawy, MD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer of Anesthesiology, Surgical Intensive Care and Pain Medicine, Faculty of Medicine, Tanta University, Tanta, Egypt.

Study Record Dates

First Submitted

September 27, 2026

First Posted

October 1, 2026

Study Start (Estimated)

October 15, 2026

Primary Completion (Estimated)

September 1, 2027

Study Completion (Estimated)

September 1, 2027

Last Updated

October 1, 2026

Record last verified: 2026-09

Data Sharing

IPD Sharing
Will share

The data will be available upon a reasonable request from the corresponding author after the end of study for one year.

Shared Documents
STUDY PROTOCOL
Time Frame
After the end of study for one year.
Access Criteria
The data will be available upon a reasonable request from the corresponding author.

Locations