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OpenTrials
Completed

NCT Number: NCT03260361

Hypnosis and MEOPA in Regional Painful Syndrome Complex

Relation between hypnosis and MEOPA on algodystrophy.

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Croix du Sud, Quint-Fonsegrives, France

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Regional Painful Syndrome Complex

Exclusion criteria

  • deaf people

Treatment and study plan

Hypnosis, kinesitherapy, MEOPA

Other

classical intervention

Other names: Hypnosis Kinesitherapy and MEOPA (HKM)

Usual practice

Other

Usual practice with treatments and physio

Primary outcomes

  1. Pain intensity measure using visual analogical ladder (EVA)

    Time frame: 3 weeks

    pain intensity is determined by patient himself on a visual analogical ladder created by Huskisson

Secondary outcomes

  1. QDSA ( Saint Antoine Pain Questions)

    Time frame: 3 weeks

    description of the type of pain

  2. SF36 (Short Form (36) Health Survey)

    Time frame: 3 weeks

    quality of life appreciation

  3. HADs

    Time frame: 3 weeks

    Hospital Anxiety and Depression Scale

Sponsors and collaborators

Lead sponsor

University Hospital, Toulouse

Other

Registry information

Official study title

Combined Therapy of Hypnosis Kinesitherapy and MEOPA in Patients With Regional Painful Syndrome Complex

Acronym: ProHKM-SDRC

Important dates

Study start
2017
Primary completion
2022
Study completion
2022
First posted
Aug 24, 2017
Registry last updated
Aug 23, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.