Study Stopped
Abandoned research
Hypnoanalgesia in Surgical and Endovenous Treatment of Varicosis
1 other identifier
observational
N/A
0 countries
N/A
Brief Summary
Endoveinous treatment of saphenous varicoses and phlebectomia of tributary veins are commonly performed under local anesthesia. Hypnoanalgesia might reduce perinterventional pain. This study has the aim to test the effectiveness of hypnoanalgesia, performed by a specialised nurse, for peri-and post-procedual pain reduction.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started Sep 2018
Shorter than P25 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 11, 2018
CompletedFirst Posted
Study publicly available on registry
July 26, 2018
CompletedStudy Start
First participant enrolled
September 2, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2018
CompletedOctober 15, 2018
December 1, 2017
29 days
January 11, 2018
October 10, 2018
Conditions
Outcome Measures
Primary Outcomes (2)
Evaluate the effects of hypnosis
Assessment of the contribution of hypnosis in patients who will be treated under local anesthesia by Laser or radiofrequency or phlebectomies for their varicose veins
on intraoperative
Evaluate the effects of hypnosis
Assessment of the contribution of hypnosis in patients who will be treated under local anesthesia by Laser or radiofrequency or phlebectomies for their varicose veins
1 day
Interventions
No intervention
Eligibility Criteria
patients treated under local anesthesia by Laser or radiofrequency or phlebectomies for their varicose veins
You may qualify if:
- patients treated under local anesthesia by Laser or radiofrequency or phlebectomies for their varicose veins
- Age of 18 and over
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
GUDRUN BOGE
University Hospital, Montpellier
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 11, 2018
First Posted
July 26, 2018
Study Start
September 2, 2018
Primary Completion
October 1, 2018
Study Completion
October 1, 2018
Last Updated
October 15, 2018
Record last verified: 2017-12