NCT03663608

Brief Summary

The main objective is to assess patient's satisfaction regarding pure local anaesthesia and without use of a tourniquet (WALANT Technique) for trigger finger release surgery.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
57

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Nov 2017

Shorter than P25 for all trials

Geographic Reach
1 country

2 active sites

Status
completed

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 Start

First participant enrolled

November 20, 2017

Completed
10 months until next milestone

First Submitted

Initial submission to the registry

September 6, 2018

Completed
4 days until next milestone

First Posted

Study publicly available on registry

September 10, 2018

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 12, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 12, 2018

Completed
Last Updated

April 5, 2022

Status Verified

April 1, 2022

Enrollment Period

12 months

First QC Date

September 6, 2018

Last Update Submit

April 4, 2022

Conditions

Trigger Finger Disorder

Outcome Measures

Primary Outcomes (1)

  • Patient satisfaction

    Patient's agreement to use WALANT for possible surgeries to come and Patient's agreement to refer WALANT to his close relatives if they were to undergo surgery

    one day after surgery

Interventions

WALANT TechniquePROCEDURE

pure local anaesthesia and without use of a tourniquet (WALANT Technique) for trigger finger release surger

Eligibility Criteria

Age18 Years+
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients with Isolated Trigger finger, diagnosis confirmed by sonography and indication of surgical release

You may qualify if:

  • Patients of age
  • Isolated Trigger finger, diagnosis confirmed by sonography and with indication of surgical release
  • Patients protected by health insurance
  • Patients who have received proper information on the current research proctol, and did not refuse to enter the study

You may not qualify if:

  • Hand vascular disorders ( History of finger replantation surgery, clinical signs of poor hand vascularization
  • Hypersensitivy to Xylocain or Adrenalin or one of it's components
  • Other surgical act planned to be performed during the same anaesthesia
  • Pregnant or Breastfeeding women
  • Patients of age and under the protection of a conservator, patients deprived of liberty

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Centre Hospitalier Privé de Plérin

Plérin, 22190, France

Location

CHU de Rennes

Rennes, 35033, France

Location

MeSH Terms

Conditions

Trigger Finger Disorder

Condition Hierarchy (Ancestors)

Tendon EntrapmentTendinopathyMuscular DiseasesMusculoskeletal Diseases

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 6, 2018

First Posted

September 10, 2018

Study Start

November 20, 2017

Primary Completion

November 12, 2018

Study Completion

November 12, 2018

Last Updated

April 5, 2022

Record last verified: 2022-04

Locations

FR(2)