Participate in a Female Sexual Arousal Disorder Clinical Study.
Are you a postmenopausal woman concerned about your libido? If so, you could be eligible to participate in a clinical trial to evaluate an investigational medication consisting of a daily intravaginal insert for 28 weeks.
To be eligible, you must:
- Be a postmenopausal woman 40 to 80 years of age;
- Meet other criteria of the clinical study
A financial compensation up to $425 may be provided upon completion of the study. This trial is sponsored by Endoceutics and has been reviewed by an independent Ethics Committee.
To learn more call our East Wichita location at 316-689-6652
Please fill out your information below and a Heartland Research specialist will contact you with more information for this study.
The information you provide is entered in our secure, password protected database. The provided information will only be used to contact you to tell you more about the study. You have the choice to have your information saved or removed from our records. If you elect to have contact information saved within our database, it will remain indefinitely. To be removed please call a Heartland Research specialist at 316-689-6626 or email firstname.lastname@example.org.