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Clinical Trials/ITMCTR2200005653
ITMCTR2200005653
Not yet recruiting
未知

Evaluation of the effects of intradermal needle therapy on sleep quality in patients following laparoscopic hysterectomy

Guangdong Hospital of traditional Chinese Medicine0 sitesTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
perioperative disease
Sponsor
Guangdong Hospital of traditional Chinese Medicine
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional study
Sex
Female

Investigators

Sponsor
Guangdong Hospital of traditional Chinese Medicine

Eligibility Criteria

Inclusion Criteria

  • Patients eligible for inclusion will be selected with reference to the Total Hysterectomy: Surgical Method for Benign Disease edited by Waters et al. (Beijing People's Military Medical Publishing House, 2012\). Briefly, study inclusion criteria will be as follows: (1\) women diagnosed with non\-malignant uterine tumors or adnexal masses, or with early\-stage tumors (including stage IA1 tumors and carcinoma in situ) that meet the surgical indications for laparoscopic total hysterectomy; (2\) individuals 18\-65 years of age; (3\) American society of anesthesiologists (ASA) grade I\-II patients, with anesthesia being achieved via tracheal intubation, an operative duration \< 4 h, and \< 300 mL of intraoperative blood loss; (4\) individuals without any history of short\-term or chronic insomnia; (5\) patients without reported preoperative mental health disorders, illnesses, or a history of substance abuse or sedative drug abuse; and (6\) patients that agree to participate in the study and provide written informed consent

Exclusion Criteria

  • Patients will be excluded from participation in the present study if they meet any of the following criteria: (1\) patients with a history of sleep disorders, mental health disorders, or sedative drug abuse; (2\) patients with severe primary or secondary diseases affecting major organs including the brain, kidney, liver, or heart; (3\) patients with local skin wounds, infections, or tape allergies at the target acupoints; (4\) patients that have participated in other clinical trials within the past year; and (5\)patients diagnosed with diabetes.

Outcomes

Primary Outcomes

Not specified

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