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Use of Metabolomics to Differentiate the Antihypertensive Effect of Acupuncture From Sham Acupuncture in Hypertensives

Use of Metabolomics to Differentiate the Antihypertensive Effect of Acupuncture From Sham Acupuncture in Hypertensives

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03492892
Enrollment
10
Registered
2018-04-10
Start date
2012-01-01
Completion date
2016-12-31
Last updated
2018-04-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension,Essential

Keywords

acupuncture, hypertension, targeted metabolome, pilot clinical trial

Brief summary

To assess the effect of acupuncture versus sham acupuncture on regulating the targeted metabolome of hypertensive patients.

Detailed description

Acupuncture has been widely used for blood pressure management. Its effect on the cardiovascular-related targeted metabolome is still unknown. This pilot study aimed to assess the effect of acupuncture versus sham acupuncture on regulating the targeted metabolome of hypertensive patients.

Interventions

DEVICEAcupuncture

Stimulate acupoint with filiform needles to restore the healthy condition of patients

DEVICESham Acupuncture

Stimulate non-acupoint with filiform needles to treat the condition of patients

Sponsors

Chengdu University of Traditional Chinese Medicine
CollaboratorOTHER
The University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
45 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* aged between 45 and 75 years; * were diagnosed as stage I hypertension in the first visit, or used to be diagnosed with stage I hypertension in recent 1 year, but without any medication history; * without neurological, other cardiovascular, hepatic and renal disease, and other visceral diseases; * the basal metabolism rate of a patient, which was measured by the retrospective dietary questionnaire at baseline, should be approximately 1:1.4; * didn't administer any drugs or herbs in at 15 days before the start of the study; * didn't participate in any study other than this; * agreed to cooperate with researchers in all research procedures after they were introduced this study; and * provided with written informed consent.

Exclusion criteria

* age≤45 or age≥75; * with hypertension which was secondary to other diseases, such as renal vascular disease, Cushing's syndrome, hyperadrenocorticism and drug-induced hypertension; * had complicated cardiovascular, digestive, respiratory, urinary, blood, nervous, endocrine system and other severe primary diseases and failed to effectively control in clinic; * accompanied by epilepsy, sleep apnea, hypopnea syndrome, etc.; * with psychiatric symptoms such as severe depression or anxiety (SAS≥70, or SDS≥72); * pregnant or lactating woman, or woman of reproductive age who was intended to conceive in recent 1 year; * with abnormality in laboratory test of blood biochemistry, or with contagious risks, such as HIV virus carrier, or patient with positive Hepatitis B Virus (HBV) superficial antigen; * with malignant tumor or other severe consuming diseases, or patients with infections or bleeding disorders; * alcoholics or drug abusers, or vegetarians; * used to suffer from acute diseases in recent 2 weeks, such as high fever, or gastritis; * used to administer any drug that may potentially impaired renal or hepatic function; * with cardiovascular disease that had been treated with acupuncture within recent three months; or * undergoing other clinical trials.

Design outcomes

Primary

MeasureTime frame
24 hour ambulatory blood pressureup to week 6

Secondary

MeasureTime frame
targeted plasma metabolomeup to week 6

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026