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Effects of Spinal Cord Injury on Female Sexual Response

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified October 2006 by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00142714
First Posted: September 2, 2005
Last Update Posted: October 16, 2006
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
September 1, 2005
September 2, 2005
October 16, 2006
August 2003
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  • Our central hypothesis are:
  • 1) In females the SNS regulates psychogenic genital vasocongestion 2) In females the orgasmic reflex requires the presence of an intact sacral spinal cord, 3) In females a pattern generator is responsible for the orgasmic reflex.
Same as current
Complete list of historical versions of study NCT00142714 on ClinicalTrials.gov Archive Site
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Effects of Spinal Cord Injury on Female Sexual Response
Effects of SCI on Female Sexual Response
The long term aims of this project are to 1) Understand the effect of varying degrees and levels of SCI and dysfunction(SCI/D)on females sexual response: 2) Identify the specific neuronal pathways involved in female sexual responses; and 3) Develop and evaluate new assessment and treatment methods for neurogenic sexual dysfunction in women.
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Interventional
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Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Educational/Counseling/Training
  • Female Sexual Dysfunction
  • Multiple Sclerosis
  • Spinal Cord Injury
Procedure: Sympathetic manipulation on sexual arousal in women
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Unknown status
70
June 2005
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Inclusion Criteria:

  • MS or SCI
  • Normal menstrual periods
  • Normal hand function
  • Have ability to feel sensation from lower abdomen to upper thigh region.

Exclusion Criteria:

  • Pregnant
  • Menopausal
Sexes Eligible for Study: Female
18 Years to 55 Years   (Adult)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00142714
5R01HD030149-09( U.S. NIH Grant/Contract )
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Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
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Principal Investigator: Marca Sipski, MD The University of Alabama at Birmingham
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
October 2006

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP