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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00379626
Other study ID # AH 048-01
Secondary ID
Status Terminated
Phase Phase 1
First received September 21, 2006
Last updated February 13, 2017
Start date August 2003
Est. completion date August 2010

Study information

Verified date February 2017
Source Norwegian University of Science and Technology
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to determine if Cognitive treatment and hormone treatment can change the relapse rate of sexual offenders.


Description:

The aim of this study is to determine if Cognitive treatment and hormone treatment can change the relapse rate of sexual offenders.

In the first part of study we are studying changes in the offenders cognitive distortions and in the second part we are studying changes in sexual activities and sexual thoughts after treatment with Leuprorelin. The study is an open pre and post study.


Recruitment information / eligibility

Status Terminated
Enrollment 5
Est. completion date August 2010
Est. primary completion date August 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

Men sentenced for paraphilia

Exclusion Criteria:

Men above 70 years and men that does not speak english

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
cognitive and hormone treatment
cognitive and hormone (Leuprorelin) treatment

Locations

Country Name City State
Norway St. Olavs Hospital. Departement for forensic psyciatry, Brøset. Trondheim

Sponsors (1)

Lead Sponsor Collaborator
Norwegian University of Science and Technology

Country where clinical trial is conducted

Norway, 

References & Publications (1)

Nøttestad JA, Bjarnar E, Lundmo PI, Sandvik M. [Treatment of sex offenders with leuprorelin]. Tidsskr Nor Laegeforen. 2006 Feb 23;126(5):633-4. Norwegian. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary The degree of cognitive distortions after treatment 8 months
Secondary Locus of control after treatment in part one. 8 months
Secondary Degree of mental health problems (SCL-90) 8 months
Secondary The testosterone levels before, during and after treatment measured each 3rd month baseline upto 8 months
See also
  Status Clinical Trial Phase
Not yet recruiting NCT05482412 - Acute Intense Paraphilic Desire (DSM-V) Down-Regulation Via taVNS Neuro-Modulation [Transcutaneous Afferent Vagus Nerve] With Future Operative Implant Consideration N/A
Not yet recruiting NCT04316650 - Study of Maintenance of the Efficiency and Adverse Effects of Pharmacological Treatments in Sex Offenders With Paraphilia N/A
Completed NCT01743209 - Descriptive Epidemiology Study for Patients With Paraphilia Sex Offenders and Receiving Androgen Antagonists N/A