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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT01562964 |
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Date of registration:
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22/03/2012 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Hypnotherapy in Patients With Chest Pain & Unobstructed Coronaries
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Scientific title:
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The Impact of Hypnotherapy on Symptoms, Psychological Morbidity and Quality of Life in Postmenopausal Women With Chest Pain and Unobstructed Coronary Arteries |
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Date of first enrolment:
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February 1, 2012 |
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Target sample size:
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0 |
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Recruitment status: |
Withdrawn |
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URL:
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https://clinicaltrials.gov/show/NCT01562964 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: None (Open Label).
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Phase:
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N/A
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Countries of recruitment
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United Kingdom
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Contacts
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Name:
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Peter Collins, MD, FRCP |
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Address:
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Telephone:
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Email:
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Affiliation:
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Imperial College London, and Royal Brompton & Harefield NHS Foundation Trust |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- history of chest pain for = 2 years
- = 2 episodes chest pain per week
- angiographically smooth epicardial coronary arteries
- Willing to give written informed consent
Exclusion Criteria:
- Any epicardial coronary atheroma on angiography of the coronary arteries
- left ventricular hypertrophy or dysfunction (clinical/ECG/echo/CXR)
- previous hypnotherapy for chest pain symptoms
- participation in research project within previous 60 days
- unwilling to give written informed consent
Age minimum:
18 Years
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Chest Pain
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Unobstructed Coronary Arteries
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Intervention(s)
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Behavioral: Supportive therapy
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Behavioral: Hypnotherapy
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Primary Outcome(s)
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Symptom frequency
[Time Frame: 24 weeks]
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Secondary Outcome(s)
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Hospitalisations
[Time Frame: 24 weeks]
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Consultancy time
[Time Frame: 24 weeks]
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General quality of life
[Time Frame: 24 weeks]
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Medication use
[Time Frame: 24 weeks]
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Symptom severity
[Time Frame: 24 weeks]
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Psychological morbidity
[Time Frame: 24 weeks]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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