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Norwegian Distal Ulna Resection - Replacement Study (NORDURR)

Primary Purpose

Osteoarthritis Wrist

Status
Recruiting
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Darrach
Prosthesis
Sponsored by
Ostfold Hospital Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoarthritis Wrist focused on measuring Distal radioulnar joint, Darrach procedure, Ulnar head resection, Herbert prosthesis, Ulnar head replacement

Eligibility Criteria

30 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • painful osteoarthritis distal radioulnar joint
  • stable DRUJ

Exclusion Criteria:

  • activ inflammatory disease with significant destruction of the joint
  • "low demand" persons
  • significant instability i DRUJ
  • active infections, poor soft tissue conditions
  • accidental wound on the operated hand
  • general contraindications for surgery

Sites / Locations

  • Innlandet Hospital Trust
  • Haukeland University Hospital
  • Oslo University HospitalRecruiting
  • University Hospital of North Norway
  • University Hospital of St Olav
  • Østfold Hospital TrustRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Darrach

Prosthesis

Arm Description

Surgical procedure: resection of distal ulna

Surgical procedure: ulnar head replacement

Outcomes

Primary Outcome Measures

Norwegian version of Quick DASH (Quick Disability Arm Shoulder Hand) score
specific patient reported outcome measure, scale with range 0-100, with 0 defined as best possible and 100 as worst possible outcome

Secondary Outcome Measures

Norwegian vesrion of PRWHE (Patient Rated Wrist Hand Evaluation) score
Hand specific patient reported outcome measure, scale with range 0-100, with 0 defined as best and 100 as worst subjective outcome
Visual Analogue Scale (VAS) pain scale
subjective evaluation of pain intensity, a scale with range 0-10 with 0 defined as best possible and 10 as worst outcome
Active range of motion
objective measurement of movements in degrees, a scale with range 0-180 degrees.
Grip strength
Measurement of grip strength of the hand, scale with range 0-100 kilograms
complications and reoperations
Registration of occurance of any adverse event, will be reported as number of participants with complications and reoperations

Full Information

First Posted
March 28, 2019
Last Updated
April 22, 2022
Sponsor
Ostfold Hospital Trust
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1. Study Identification

Unique Protocol Identification Number
NCT04074863
Brief Title
Norwegian Distal Ulna Resection - Replacement Study
Acronym
NORDURR
Official Title
Norwegian Distal Ulna Resection vs. Replacement Study. A Prospective Randomized Multicenter Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 16, 2020 (Actual)
Primary Completion Date
December 31, 2029 (Anticipated)
Study Completion Date
December 31, 2029 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ostfold Hospital Trust

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Osteoarthritis of the joint between the forearm bones at the wrist (distal radioulnar joint, DRUJ) is a common sequel of fracture and ligament injuries or degenerative disease of the wrist. Intact DRUJ is important for normal load transfer from the hand to the forearm. DRUJ osteoarthritis leads to pain and decreased lifting capacity and rotation of the forearm. The standard treatment is resection of the ulnar head, known as the Darrach procedure. After the resection there is no longer contact in the affected joint, however, some patients can experience instability or impingement between the forearm bones. With ulnar head implant replacement may the load transfer and the stability between the forearm bones less affected. Studies with good long term results are published with both resection and replacement. However, these methods were never compared and thus it is not clear, which of the methods gives the best clinical result and less complications. The aim of this study is to compare Darrach procedure with ulnar head replacement in a prospective randomized multicenter study. Several hand surgical centers form Norway would participate this study. Individuals seeking treatment for their stable but painful DRUJ joints will be included and randomized to either Darrach procedure or ulnar head implant. Participants will be followed up to 5 years. Range of motion and grip strength measures and functional scores would be registered before operation, after 3 months, 1 and 5 years. Eventual complications and reoperations would be also registered.
Detailed Description
Osteoarthritis of the joint between the forearm bones at the wrist (distal radioulnar joint, DRUJ) is a common sequel of fracture and ligament injuries or degenerative disease of the wrist. Intact DRUJ is important for normal load transfer from the hand to the forearm. DRUJ osteoarthritis leads to pain and decreased lifting capacity and rotation of the forearm. The standard treatment is resection of the ulnar head, known as the Darrach procedure. After the resection there is no longer contact in the affected joint, however, some patients can experience instability or impingement between the forearm bones. With ulnar head implant replacement may the load transfer and the stability between the forearm bones less affected. Studies with good long term results are published with both resection and replacement. However, these methods were never compared and thus it is not clear, which of the methods gives the best clinical result and less complications. The aim of this study is to compare Darrach procedure with ulnar head replacement in a prospective randomized multicenter study. The study would be coordinated from Østfold Hospital Trust, and Oslo University Hospital, Haukeland University Hospital, Innlandet Hospital Trust, University Hospital of St Olav and University Hospital of North Norway would participate this study. Participants would be included among individuals seeking treatment for their stable but painful DRUJ joints. Informed consent will be gained from every participant. The group size was calculated to 20 participants in both groups. Participants will be randomized to either Darrach procedure or ulnar head implant. The procedures would be carried out standardized in every center. No further stabilization procedure for the ulna stump would be used in resection. Herbert UHP implant (Herbert Ulnar Head Prosthesis, KLS Martin, Germany) would be used for ulnar head replacement. Postoperative treatment and follow up would be identical between the groups. Range of motion and grip strength measures and functional scores would be registered by an independent hand therapist before operation, after 3 months, 1 and 5 years. Eventual complications and reoperations would be also registered. Patient related outcome measure scores, range of motion and grip strength would be registered as outcomes. The results would be checked for normal distribution and either parametric or non parametric statistical tests would be chosen for comparison of the two groups. The null hypothesis is that Darrach procedure and ulnar head replacement with implant gives similar functional results, similar frequency of complication and reoperations.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis Wrist
Keywords
Distal radioulnar joint, Darrach procedure, Ulnar head resection, Herbert prosthesis, Ulnar head replacement

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants randomized to one of the group and receive the group specific surgery. Postoperative treatment is identical between the groups.
Masking
Outcomes Assessor
Masking Description
An independent hand therapist, who is not involved in the rehabilitation of the participants, will carry out the measurements.
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Darrach
Arm Type
Active Comparator
Arm Description
Surgical procedure: resection of distal ulna
Arm Title
Prosthesis
Arm Type
Active Comparator
Arm Description
Surgical procedure: ulnar head replacement
Intervention Type
Procedure
Intervention Name(s)
Darrach
Other Intervention Name(s)
resection of ulnar head (Darrach procedure)
Intervention Description
Surgical treatment of painful DRU osteoarthritis with resection of distal ulna
Intervention Type
Procedure
Intervention Name(s)
Prosthesis
Other Intervention Name(s)
Herbert disltal ulna implant
Intervention Description
Surgical treatment of painful DRU osteoarthritis with distal ulna replacement with Herbert implant
Primary Outcome Measure Information:
Title
Norwegian version of Quick DASH (Quick Disability Arm Shoulder Hand) score
Description
specific patient reported outcome measure, scale with range 0-100, with 0 defined as best possible and 100 as worst possible outcome
Time Frame
at 5 years
Secondary Outcome Measure Information:
Title
Norwegian vesrion of PRWHE (Patient Rated Wrist Hand Evaluation) score
Description
Hand specific patient reported outcome measure, scale with range 0-100, with 0 defined as best and 100 as worst subjective outcome
Time Frame
at 5 years
Title
Visual Analogue Scale (VAS) pain scale
Description
subjective evaluation of pain intensity, a scale with range 0-10 with 0 defined as best possible and 10 as worst outcome
Time Frame
at 5 years
Title
Active range of motion
Description
objective measurement of movements in degrees, a scale with range 0-180 degrees.
Time Frame
at 5 years
Title
Grip strength
Description
Measurement of grip strength of the hand, scale with range 0-100 kilograms
Time Frame
at 5 years
Title
complications and reoperations
Description
Registration of occurance of any adverse event, will be reported as number of participants with complications and reoperations
Time Frame
at 5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: painful osteoarthritis distal radioulnar joint stable DRUJ Exclusion Criteria: activ inflammatory disease with significant destruction of the joint "low demand" persons significant instability i DRUJ active infections, poor soft tissue conditions accidental wound on the operated hand general contraindications for surgery
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Istvan Zoltan Rigo, PhD
Phone
+47 69860000
Email
istvan.zoltan.rigo@so-hf.no
First Name & Middle Initial & Last Name or Official Title & Degree
Jan-Ragnar Haugstvedt, PhD
Phone
+47 69860000
Email
Jan-Ragnar.Haugstvedt@so-hf.no
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Istvan Zoltan Rigo, PhD
Organizational Affiliation
Ostfold Hospital Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Innlandet Hospital Trust
City
Lillehammer
State/Province
Oppland
ZIP/Postal Code
2629
Country
Norway
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ole Anton Kragh Fosse, MD
Phone
915 06 200
Email
ole.a.k.fosse@sykehuset-innlandet.no
Facility Name
Haukeland University Hospital
City
Bergen
ZIP/Postal Code
5021
Country
Norway
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Eivind Strandenes, MD
Phone
55972771
Email
eivind.strandenes@helse-bergen.no
Facility Name
Oslo University Hospital
City
Oslo
ZIP/Postal Code
0424
Country
Norway
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Magne Røkkum, PhD, Prof
Phone
+4723070000
Email
mrokkum@ous-hf.no
First Name & Middle Initial & Last Name & Degree
Sondre Hasselllund, MD
Phone
+4722118080
Email
sondre.hassellund@gmail.com
Facility Name
University Hospital of North Norway
City
Tromsø
ZIP/Postal Code
9038
Country
Norway
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hebe Desiree Kvernmo, PhD, Prof
Phone
776 26000
Email
hebe.kvernmo@gmail.com
Facility Name
University Hospital of St Olav
City
Trondheim
ZIP/Postal Code
7006
Country
Norway
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Heike Brigitta Zeitlemann, MD
Phone
+4772826000
Email
heike.zeitlmann@stolav.no
Facility Name
Østfold Hospital Trust
City
Moss
State/Province
Østfold
ZIP/Postal Code
1535
Country
Norway
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Istvan Zoltan Rigo, PhD
Phone
+4769860000
Email
istvan.zoltan.rigo@so-hf.no
First Name & Middle Initial & Last Name & Degree
Jan-Ragnar Haugstvedt, PhD
Phone
+4769860000
Email
jan-ragnar.haugstvedt@so-hf.no

12. IPD Sharing Statement

Plan to Share IPD
No

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Norwegian Distal Ulna Resection - Replacement Study

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