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. Author manuscript; available in PMC: 2011 Oct 12.
Published in final edited form as: Cochrane Database Syst Rev. 2009 Oct 7;(4):CD006690. doi: 10.1002/14651858.CD006690.pub2
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