NCT07814989

Brief Summary

Rheumatoid arthritis is a chronic, systemic, autoimmune inflammatory disease that mainly affects the joints and periarticular soft tissues.\[1\]

Trial Health

63
Monitor

Trial Health Score

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

Enrollment
180

participants targeted

Target at P75+ for not_applicable

Timeline
9mo left

Started Aug 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

Study Progress16%
Aug 2026Jul 2027

Study Start

First participant enrolled

August 15, 2026

Completed
15 days until next milestone

First Submitted

Initial submission to the registry

August 30, 2026

Completed
12 days until next milestone

First Posted

Study publicly available on registry

September 11, 2026

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2027

Expected
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2027

Last Updated

September 11, 2026

Status Verified

July 1, 2026

Enrollment Period

5 months

First QC Date

August 30, 2026

Last Update Submit

September 6, 2026

Conditions

Keywords

Rheumatoid ArthritisNerve blockWrist injection

Outcome Measures

Primary Outcomes (2)

  • Change in wrist pain severity measured by the Visual Analogue Scale (VAS) from baseline to Week 16

    Change in wrist pain severity measured using the Visual Analogue Scale (VAS) from baseline to Week 16 Visual Analogue Scale (VAS), ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Wrist pain severity will be assessed using the Visual Analogue Scale (VAS), ranging from 0 to 10, where 0 represents no pain and 10 represents the worst imaginable pain. Higher scores indicate greater pain. The change in VAS score from baseline to Week 16 will be assessed.

    Baseline to Week 16

  • Assessment of wrist pain improvement

    • Change in wrist pain severity measured by the Visual Analogue Scale (VAS) from baseline to Week 16

    16 weeks

Study Arms (3)

Group 1

ACTIVE COMPARATOR

wrist nerve block

Procedure: Wrist local steroid injection

Group 2

PLACEBO COMPARATOR

wrist local steroid injection

Procedure: Wrist local steroid injection

Group 3

NO INTERVENTION

Interventions

Wrist nerve block by injection is a diagnostic or therapeutic procedure used to treat chronic wrist pain, typically arising from arthritis or instability, by interrupting sensory nerve signals (mainly PIN/AIN nerves) with an anesthetic or neurolytic agent. This less-invasive approach provides pain relief, often serving as a predictor for success before permanent surgical denervation.\[4\]

Group 1Group 2

Eligibility Criteria

Age16 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • RA patients fulfilled the 2010 American College of Rheumatoid Arthritis classification criteria.\[8\]
  • Oligoarticular RA patients including wrist joint.
  • Age above 18 years old.
  • Patient cooperative and can answer questions.

You may not qualify if:

  • Other rheumatologic or collagen diseases.
  • Age below 18 years.
  • Patients who underwent concomitant procedures to address underlying pathology such as radial styloidectomy, ulna shortening, fracture fixation, arthroplasty, arthrodesis, and ligament reconstructions.
  • Patients who suffered from hand deformities or limitation.
  • Uncooperative patients.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sohag University Hospital

Sohag, Egypt

Location

MeSH Terms

Conditions

Arthritis, Rheumatoid

Condition Hierarchy (Ancestors)

ArthritisJoint DiseasesMusculoskeletal DiseasesRheumatic DiseasesConnective Tissue DiseasesSkin and Connective Tissue DiseasesAutoimmune DiseasesImmune System Diseases

Central Study Contacts

Youssra Ali Resident

CONTACT

Ahmed mahrous elsamman

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Resident

Study Record Dates

First Submitted

August 30, 2026

First Posted

September 11, 2026

Study Start

August 15, 2026

Primary Completion (Estimated)

January 1, 2027

Study Completion (Estimated)

July 1, 2027

Last Updated

September 11, 2026

Record last verified: 2026-07

Locations