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Assessment of Energetic Resonance by Cutaneous Stimulation on Withdrawal Alcohol Symptoms. (RESC)

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Civil Hospices of Lyon

Status

Completed

Conditions

Alcohol Withdrawal Syndrome

Treatments

Other: Energetic Resonance by Cutaneous Stimulation

Study type

Interventional

Funder types

Other

Identifiers

NCT02146716
2013-840

Details and patient eligibility

About

The purpose of RESC study is to assess the efficacy of Energetic Resonance by Cutaneous Stimulation on alcohol withdrawal symptoms measured by CUSHMAN score and in a second time to measure the benzodiazepine amount prescribed during the withdrawal time.

Enrollment

43 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Men and women between 18 and 80 years,
  • Patient with alcohol addiction,
  • Patient needing alcohol withdrawal in a hospital.
  • Patient with social Security,
  • Patient with inform consent signed.

Exclusion criteria

  • Pregnant women
  • Minor.
  • Major with guardianship.
  • People without sufficient information because of troubles of cognitive functions, or without sufficient knowledge of French language.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

43 participants in 2 patient groups

Control
No Intervention group
Energetic Resonance by Cutaneous Stimulation
Experimental group
Description:
Energetic Resonance by Cutaneous Stimulation session in addition to standard treatment for patients with withdrawal alcohol symptoms.
Treatment:
Other: Energetic Resonance by Cutaneous Stimulation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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