FindTrial
Sign In

Management of trigger fingers

TRIGGER Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON22206
Enrollment
Unknown
Registered
2017-09-28
Start date
2018-01-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Trigger finger Tendovaginitis stenosans TVS

Interventions

Surgical release using surgeon’s preferred technique (open or percutaneous)

Sponsors

Primary: RSTN (Reconstructive Surgery Trails Network, UK) Secundary: - Oxford Trials Unit - Jeroen Bosch Hospital - UMC Utrecht - NVPC (Dutch Society Plastic Surgeons) - ICOPLAST (network for European trainees in plastic surgery) - NVVH (Dutch Society Hand Surgeons)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • One or more trigger fingers • Grade 1-3 trigger finger (according to classification by Quinnell) • Participation is voluntary and with informed consent

Exclusion criteria

Exclusion criteria: • Aged <18 • Congenital trigger finger • Mentally disabled persons • Grade 4 trigger finger (according to classification by Quinell) • Allergy for corticosteroids • Previous surgical release for triggering • Previous injection therapy • History of surgical intervention in the same digit

Design outcomes

Primary

MeasureTime frame
Resolution of triggering (recurrence rate)—

Secondary

MeasureTime frame
Level of pain (NRS-score), hand function (patient related outcome measure), costs and complications—

Contacts

Public ContactA. Dijksterhuis
triggertrial@gmail.com+31 6 53396563

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)