Methods | Parallel randomised controlled trial |
Participants | SETTING: Hospital outpatients and patients recruited from general company check-up; Shugang Hospital, Shanghai, China |
WHO PARTCIPATED: 42 (22 in the intervention group, M/F 8/14; and 20 in the control group M/F 8/12) | |
INCLUSION CRITERIA: IGT (WHO 1985) | |
EXCLUSION CRITERIA: disorders that interfere with glucose metabolism | |
CO-MORBIDITIES: none reported | |
CO-MEDICATIONS: none reported | |
Interventions | INTERVENTION: Tangheng I, 2 bags twice a day for 3 mth splus lifestyle modification (diet & exercise) |
CONTROL: lifestyle modification (diet and exercise) for 3 months | |
Outcomes | FBG (mmol/L), 2hr-GTT (mmol/L), insulin (ng/mL), BMI, systolic blood pressure (mmHg), diastolic blood pressure (mmHg) |
All outcomes were assessed at baseline and trial completion (3 months) | |
Study details | DURATION OF INTERVENTION: 3 months |
DURATION OF FOLLOW-UP: 3 months | |
RUN-IN PERIOD: none | |
Publication details | LANGUAGE OF PUBLICATION: Chinese |
COMMERCIAL FUNDING: no | |
NON-COMMERCIAL FUNDING: no | |
PUBLICATION STATUS (PEER REVIEW JOURNAL): yes | |
PUBLICATION STATUS (JOURNAL SUPPLEMENT): no | |
PUBLICATION STATUS (ABSTRACT): yes | |
Stated aim of study | Quote “To observe the intervention on 42 cases of impaired glucose with Tangheng I.” |
Notes |