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The effect of transversus abdominis plane block combined with paracetamol injection on postoperative analgesia and sleep quality after laparoscopic total hysterectomy

The effect of transversus abdominis plane block combined with paracetamol injection on postoperative analgesia and sleep quality after laparoscopic total hysterectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092994
Enrollment
Unknown
Registered
2024-11-27
Start date
2024-12-02
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

None

Interventions

Ariyan group:The intervention phase totaled 24h, with medication administered every 8 hours based on grouping results. After subjects entered the preoperative preparation room on the day of surgery, p
Placebo group:The intervention phase lasted 24 h, and the drugs were administered every 8 h according to the grouping results. After subjects entered the preoperative preparation room on the day of su

Sponsors

Zhongshan Hospital of Fudan University, Xiamen Branch
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: a. Age: 18-70 years old b, Type of surgery: laparoscopic total hysterectomy c, ASA classification: Grade I-III d, able to use pain scale, QoR-15 scale, sleep quality scale and operate intravenous PCA device e, Understanding and willingness to participate in the trial, signed informed consent by themselves or their immediate family members

Exclusion criteria

Exclusion criteria: a. Clear preoperative allergy or hypersensitivity to test drugs (acetaminophen and mannitol); b. Impairment of vital organs such as impaired liver function (transaminases = twice the upper limit), patients with active liver disease, chronic hepatitis, cirrhosis of the liver, chronic kidney disease, renal insufficiency (creatinine = 2.0 mg/dl), chronic malnutrition, and known or suspected history of alcohol or drug abuse; c. Pregnant or lactating patients; d. Those who require preoperative sleep aids with tranquilizers; e. severe hypovolemia (due to dehydration or blood loss), glucose-6-phosphatase dehydrogenase deficiency; f. The presence of trauma, infection or dermatitis at the puncture site that precludes nerve block operation; g. patients with preoperative cognitive dysfunction.

Design outcomes

Primary

MeasureTime frame
Pain visual analog score;QoR-15;Sleep quality score;

Secondary

MeasureTime frame
Postoperative opioid consumption;rescue analgesia rate;Incidence of anesthesia-related adverse reactions;Antiemetic rescue rate;

Countries

China

Contacts

Public ContactGuiting Li

Zhongshan Hospital of Fudan University, Xiamen Branch

GuitingLiA@163.com+86 158 5925 8501

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026