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Outcomes of Motion-preserving Surgery and Arthrodesis at the Distal Interphalangeal (DIP) Joint

S

Schulthess Klinik

Status

Completed

Conditions

Distal Interphalangeal Arthrodesis
Distal Interphalangeal Arthroplasty

Treatments

Device: DIP arthroplasty or arthrodesis

Study type

Observational

Funder types

Other

Identifiers

NCT03074916
DIP_Silicone_retro

Details and patient eligibility

About

The objective of this project is to investigate the subjective and clinical outcome in patients at least one year after DIP arthroplasty and compare them to matched patients with an arthrodesis.

The primary endpoint is the satisfaction with the treatment result of in the motion-preserving DIP surgery at follow-up.

Enrollment

52 patients

Sex

All

Ages

18 to 111 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Arthroplasty group:

  • DIP silicone arthroplasty at least one year ago
  • Informed consent as documented by signature

Arthrodesis group:

  • Matched patients with an DIP arthrodesis
  • Informed consent as documented by signature

Exclusion criteria

Arthroplasty group:

  • Silicone arthroplasty at the thumb IP joint
  • Major surgery at another joint (PIP arthroplasty, thumb trapeziectomy) less than 6 months ago
  • Legal incompetence
  • German language barrier to complete the questionnaires

Arthrodesis group:

  • Arthroplasty at another DIP joint
  • Major surgery at another joint (PIP arthroplasty, thumb trapeziectomy) less than 6 months ago
  • Legal incompetence
  • German language barrier to complete the questionnaires

Trial design

52 participants in 2 patient groups

DIP arthroplasty
Treatment:
Device: DIP arthroplasty or arthrodesis
DIP arthrodesis
Treatment:
Device: DIP arthroplasty or arthrodesis

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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