Condition 1: Sleep quality. Condition 2: Postoperative Pain. Other sleep disorders not due to a substance or known physiological condition Other acute postprocedural pain
Conditions
Interventions
Intervention 1: Intervention group: Administration of an oral solution (as drops) of cannabidiol at a concentration of 100 mg/mL and a dose of 25 mg (equivalent to 0.25 mL of the solution) will be giv
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Patients Undergoing Intermediate Elective Abdominal Surgery Age between 18 and 65 years American Society of Anesthesiologists (ASA class) II/III Patient satisfaction
Exclusion criteria
Exclusion criteria: Addicted patients Patients with a history of psychiatric disorders and sleep disturbances
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Post operative sleep quality. Timepoint: Once after the intervention (after recovery). Method of measurement: Using the Richards-Campbell Sleep Questionnaire (RCSQ).;Post operative pain. Timepoint: At four time points: namely 1 hour, 2 hours, 4 hours, and 8 hours after the intervention. Method of measurement: Visual Analog Survey Scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactKasra Karvandian
Tehran University of Medical Sciences
Outcome results
None listed