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Clinical study of electroacupuncture in enhanced recovery of patients during peri-operative period

Phase 1
Completed
Conditions
angiocardiopathy
Registration Number
ITMCTR2000003165
Lead Sponsor
Guizhou Provincial People's Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

(1) patients undergoing cardiac valve replacement under cardiopulmonary bypass.
(2) American Society of Anesthesiology (ASA) grade II-III.
(3) Aged 18 ~ 60 years;
(4) Sign informed consent with the patient and/or his agent.

Exclusion Criteria

(1) had suffered from serious renal and ureteral diseases.
(2) had suffered from cerebrovascular diseases, epilepsy and neuropsychosis.
(3) suffering from severe heart failure and arrhythmia.
(4) has severe liver and renal dysfunction.
(5) had undergone a second operation.
(6) received acupuncture treatment recently.
(7) Hb < 120g/L for male (< 110g/L for female) and hematocrit (HCT) < 35% preoperative .
(8) the estimated CPB time may exceed 120 minutes.
(9) unexpected secondary thoracotomy occurred after surgery.
(10) patients could not tolerate acupuncture.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
urinary neutrophil gelatinase-associated lipid carrier protein;blood neutrophil gelatinase-associated lipid carrier protein;
Secondary Outcome Measures
NameTimeMethod
urea nitrogen;serum Cystatin C;serum creatinine;
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