Last updated 7 months ago

Cannabidiol for the Treatment of Pelvic Pain in Endometriosis (DREAMLAND)

102 patients around the world
Available in Brazil
The Dreamland study is a two-arm, parallel-group, individually randomized (1:1 allocation ratio), controlled by disease stage, participant and investigator blinded, single-site superiority trial of oral cannabis extract (CBD). CBD will be given orally starting at 10 mg daily and up-titrated to a maximum dose of 150 mg daily. Dose up-titration will be based on clinical response or side effects, whichever comes first. After 63 days of treatment, gradual withdrawal will be performed during one week. Then, at 70 days, there will be an open-label extension wherein all participants from control group will be offered a course of CBD according to the same previous protocol. This research intends to : 1. Assess whether the daily use of CBD, for nine weeks, will reduce the pain level of these women. 2. Assess whether the daily use of CBD, for nine weeks, will modify pain threshold. 3. Assess whether the daily use of CBD, for nine weeks, will interfere in psychological symptoms. 4. Assess the possible adverse effects of using CBD
University of Sao Paulo
1Research sites
102Patients around the world

Requirements for the patient

From 18 Years
Female

Medical requirements

Women with chronic pelvic pain secondary to endometriosis surgically treated, with refractory symptoms, and who are taking complementary hormone therapy; Women over 18 years of age who wish to participate in the clinical trial; Willingness to voluntarily participate in the study to accept randomization to either of the two treatment arms; Participating exclusively in this clinical trial during the study period; Possess a telephone (cell or landline) that may be available to receive daily calls throughout the study period; Signature of the Free and Informed Consent Term (TCLE) approved by the Local Research Ethics Committee.
Chronic, severe or uncompensated medical conditions, such as: insulin-dependent diabetes (types 1 or 2); uncontrolled high blood pressure, lung disease such as asthma or other chronic obstructive pulmonary disease; hematological diseases, liver diseases, chronic kidney disease in advanced stage (grade 3, 4 and 5), metabolic disturbances and immunosuppression; Use of any medication with potential interaction with CBD/THC (such as chloroquine, clobazan, warfarin, or valproic acid) or history of undesirable reactions prior to the use of this medications; Inability to use oral medication; Pregnancy or lactation; History of alcohol or drug addiction; Smoking in the last three years; Marijuana use in the past three months or a lifetime history of dependence; Inability to cooperate with investigators due to cognitive impairment or mental status.

Sites

Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo
Recruiting
Campus Universitário S/N, Bloco G Subsolo II, Monte Alegre, Ribeirão Preto, Sao Paulo
LinkedinInstagramFacebook
Terms and ConditionsPrivacy Policy