Skip to content

Functional Recovery Following Orthopedic Wrist Surgery Under Peripheral Nerve Block Versus General Anesthesia

Prospective Cohort Study Comparing Functional Recovery Following Orthopedic Wrist Surgery Under Peripheral Nerve Block Versus General Anesthesia

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04541745
Acronym
FUNCTION
Enrollment
72
Registered
2020-09-09
Start date
2019-08-30
Completion date
2021-12-31
Last updated
2023-01-06

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

Conditions

Recovery of Function

Keywords

Upper limb surgery, Functional recovery, Postoperative recovery, General anesthesia, Brachial plexus, Nerve block, Regional anesthesia, Peripheral anesthesia

Brief summary

This study aims at determining if there is an association between locoregional anesthesia and postoperative functional recovery for orthopedic surgery to repair a distal radial fracture, as compared to general anesthesia.

Detailed description

All patients undergoing orthopedic wrist surgery under locoregional or general anesthesia at the CIUSSS de l'Estrie-CHUS who meet the selection criteria will be approach to participate in this prospective single-center observational study. Using the visual analog scale and anesthesia scale, the pain and the satisfaction of the patient will be evaluated respectively 2 weeks postoperatively. At the second visit, 6 to 8 weeks postoperatively, the participant will complete the QuickDASH questionnaire to evaluate his functional recovery and the participant's pain will be reassessed with the visual analogue scale. Finally, 12 weeks postoperatively, the wrist-joint range of motion and grip-strength test results will be recorded. The participant will also be asked to complete the QuickDASH and PRWE (Patient-Rated Wrist Evaluation) questionnaires to reevaluate his functional recovery.

Interventions

None listed

Sponsors

Université de Sherbrooke
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* 18 years old and more * American Society of Anesthesiologists (ASA) score I, II, or III * Single distal radial fracture with or without ulna involvement * Orthopedic surgery by open reduction of the wrist for a distal radial fracture with or without ulnar involvement

Exclusion criteria

* Active pregnancy * Surgery with combined anesthesia (locoregional and general) * Locoregional anesthesia with catheter insertion for postoperative analgesia * Individuals with chronic pain as defined by preexisting neuropathy of the operated arm, preexisting radiculopathy of the operated limb, complex regional pain syndrome, or fibromyalgia * Polytrauma * Inability to consent

Design outcomes

Primary

MeasureTime frameDescription
Functional recovery using the grip strenght12 weeks post-surgeryWe evaluate the grip strength with JAMAR hydraulic hand dynamometer. The participant squeezes the device as hard as they can. We averaged three values on both sides.
Functional recovery using the QuickDASH (Quick Disabilities of Arm, Shoulder and Hand) questionnaire12 weeks post-surgeryThe QuickDASH assess the functional recovery. It consists of 11 questions scored from 1 to 5 (1 = no difficulty to 5 = unable). Higher scores indicate a greater level of disability.
Functional recovery using the PRWE (Patient Rated Wrist Evaluation) Questionnaire12 weeks post-surgeryThe PRWE (Patient Rated Wrist Evaluation) Questionnaire assess the pain and the persistence of functional difficulty in activities of daily living following wrist surgery. It consists of 15 questions, each rated on a scale from 0 to 10. Five questions deal specifically with pain and are rated as 0 (no pain) to 10 (worse pain); 10 questions are on functional recovery, rated from 0 (no difficulty) to 10 (unable to do). Higher scores on the subscales represent greater pain or functional disability.
Functional recovery using the range of motion of all movement of the wrist12 weeks post-surgeryWe evaluate the range of motion of all movement of the wrist with a goniometer

Secondary

MeasureTime frameDescription
Pain- 2 weeks2 weeks post-operativePost-operative pain score on the visual analogue scale. It is a 10 cm line on which the patient indicate their level of pain between 0 cm (no pain) and 10 cm (worst pain of their life).
Pain - 6 weeks6 weeks post-operativePost-operative pain score on the visual analogue scale. It is a 10 cm line on which the patient indicate their level of pain between 0 cm (no pain) and 10 cm (worst pain of their life).
Functional recovery at 6 weeks6 weeks post-operativeFunctional recovery following an orthopedic surgery under peripheral nerve block versus general anesthesia using the QuickDASH (The Quick Disabilities of Arm, Shoulder and Hand). The questionnaire consists of 11 questions scored from 1 to 5 (1 = no difficulty to 5 = unable). When all the questions are answered, the questionnaire calculate a percentage of disability. Higher scores indicate a greater level of disability.
Patient satisfaction2 weeks post-operativeSatisfaction score on the visual analogue scale. It is a 10 cm line on which the patient indicate their level of satisfaction between 0 cm (not satisfied) and 10 (fully satisfied).

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026