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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03397212
Other study ID # 59065
Secondary ID
Status Not yet recruiting
Phase Phase 4
First received November 29, 2017
Last updated January 5, 2018
Start date January 15, 2018
Est. completion date January 15, 2024

Study information

Verified date January 2018
Source Rigshospitalet, Denmark
Contact Romanas Polianskis, MD
Phone +45 35455233
Email romanas.polianskis@regionh.dk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This project aims at examining the following hypotheses:

- Treatment with NADA and clonidine reduces intensity of withdrawal symptoms to a greater extent than treatment with clonidine.

- Opioid withdrawal improves pain, physical and mental functioning and reduces opioid consumption 3 months and 1 year after withdrawal.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 50
Est. completion date January 15, 2024
Est. primary completion date January 15, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Chronic pain patients treated with opioids over 3 months

- The patient's doctor or nurse assesses that there is an indication to opioid withdrawal and / or the patient wishes to withdraw.

- The patient is motivated for opioid withdrawal

- The patient has experienced withdrawal symptoms

- The patient must be able to understand, speak and write Danish

- The patient must be able to transport himself to the pain center

Exclusion Criteria:

- Children under 18 years old

- External ear infection

- Treatment with benzodiazepines.

- Active substance abuse and alcohol abuse.

- Contraindications for treatment with clonidine:

- Allergy

- Bradyarrhythmias caused by diseased sinus cube or AV block of 2nd or 3rd grade.

- lactose intolerance

- Heart failure

- High medullary damage

- Cardiac conduction disturbances

- Pregnancy and breastfeeding

Study Design


Intervention

Other:
NADA acupuncture
Ear acupuncture protocol described by National Acupuncture Detoxification Association
Sham acupuncture
Ear acupuncture using inactive sham points

Locations

Country Name City State
Denmark Rigshospitalet Copenhagen

Sponsors (1)

Lead Sponsor Collaborator
Rigshospitalet, Denmark

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in intensity of withdrawal symptoms Change in intensity of withdrawal symptoms assessed with Danish withdrawal symptom questionnaire 3 months and 1 year
Secondary Change in quality of life assessed with SF36 Change in quality of life assessed with SF36 3 months and 1 year
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