Angelica Sinensis for the Treatment of Hot Flashes in Men Undergoing LHRH Therapy for Prostate Cancer

Sponsor
Lawson Health Research Institute (Other)
Overall Status
Completed
CT.gov ID
NCT00199485
Collaborator
St. Joseph's Health Care London (Other)
44
1
2
68
0.6

Study Details

Study Description

Brief Summary

Men undergoing androgen deprivation therapy for prostate cancer may experience significant side effects including symptoms of intense heat, facial flushing, and sweating. These so-called hot flashes are similar to those experienced by women during menopause. A traditional Chinese herbal preparation, Dong Quai, has been used for thousands of years to reduce the incidence and severity of hot flashes. Anecdotal evidence exists to support the use of Dong Quai in men treated with androgen deprivation therapy for prostate cancer.

Recently, the awareness and use of herbal remedies and over-the-counter preparations for a number of different conditions have increased dramatically. This trial was, therefore, designed to determine if Dong Quai significantly reduces the incidence and severity of hot flashes in men following androgen deprivation therapy for prostate cancer.

Condition or Disease Intervention/Treatment Phase
  • Drug: Angelica Sinensis
Phase 4

Study Design

Study Type:
Interventional
Anticipated Enrollment :
44 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
Angelica Sinensis for the Treatment of Hot Flashes in Men Undergoing Androgen Deprivation Therapy for Prostate Cancer
Study Start Date :
Oct 1, 2002
Actual Primary Completion Date :
Jun 1, 2008
Actual Study Completion Date :
Jun 1, 2008

Arms and Interventions

Arm Intervention/Treatment
Experimental: 1

Angelica Sinensis

Drug: Angelica Sinensis
Angelica Sinensis / placebo

Placebo Comparator: 2

placebo

Drug: Angelica Sinensis
Angelica Sinensis / placebo

Outcome Measures

Primary Outcome Measures

  1. assess bone loss in men with prostate cancer being treated with LHRH [at each of 3 follow up visits]

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Prostate cancer treated with some form of androgen deprivation therapy for at least one month. This includes either surgical (bilateral orchidectomy) or medical (LHRH agonist, pure or steroidal antiandrogen or combined) castration;

  • Greater than seven vasomotor episodes per week;

  • Significantly bothersome symptoms associated with these vasomotor episodes, which produce a desire in the patient to seek treatment to reduce both their incidence and severity;

  • Documented informed consent to participate in the trial.

Exclusion Criteria:
  • Enrolment in any other clinical trial or study protocol;

  • Presence of pain due to prostate cancer;

  • Life expectancy less than three months;

  • Any severe concomitant condition that would make it undesirable, in the clinician's opinion, or the subject to participate in the trial or would jeopardize compliance with the trial protocol;

  • Concomitant anticoagulation therapy or history of bleeding disorder or blood dyscrasia;

  • Known hypersensitivity to Dong Quai.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Urology Clinic & Prostate Centre, St. Joseph's Hospital, St. Joseph's Health Care London London Ontario Canada N6A 4V2

Sponsors and Collaborators

  • Lawson Health Research Institute
  • St. Joseph's Health Care London

Investigators

  • Principal Investigator: Hassan Razvi, MD, FRCSC, Urology, St. Joseph's Hospital, University of Western Ontario

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00199485
Other Study ID Numbers:
  • S-01-007
  • 08217
First Posted:
Sep 20, 2005
Last Update Posted:
Jul 29, 2008
Last Verified:
Jul 1, 2008
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 29, 2008