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Satisfaction Assessment After Axillary Block (Qual'AXI)

C

Centre Hospitalier Universitaire de Besancon

Status

Unknown

Conditions

Satisfaction, Patient

Treatments

Other: perioperative satisfaction assessment

Study type

Observational

Funder types

Other

Identifiers

NCT04305847
P/2020/480

Details and patient eligibility

About

Satisfaction assessment at 24 and 48 hours post operatively, after Axillary Brachial Plexus Block for Distal Arm Surgery.

Full description

Inclusion after distal Arm Surgery performed under Axillary Brachial Plexus Block.

Satisfaction assessment at 24 and 48 hours post operatively by self-administered survey questionnaire based on different scales: Evan-LR, Net Promotor Score, Satisfaction score.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients for whom distal arm surgery was performed under Axillary Brachial Plexus Block

Exclusion criteria

  • Refusal, inability to consent
  • inability to fill self-administered survey questionnaire
  • pregnancy and breastfeeding
  • surgery > 2 hours
  • second surgical site requiring anaesthesia or analgesia
  • chronic use of analgesia (including opioids) or illegal drugs

Trial design

200 participants in 1 patient group

Qual'AXI group
Description:
patients for whom distal arm surgery was performed under Axillary Brachial Plexus Block
Treatment:
Other: perioperative satisfaction assessment

Trial contacts and locations

1

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Central trial contact

Francis Berthier, MD

Data sourced from clinicaltrials.gov

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