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Effects of perioperative carbohydrate supplementation and postoperative analgesia on postoperative recovery of patients with cervical cancer under ERAS' concept

Effects of perioperative carbohydrate supplementation and postoperative analgesia on postoperative recovery of patients with cervical cancer under ERAS' concept

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200062036
Enrollment
Unknown
Registered
2022-07-20
Start date
2022-10-01
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Cervical cancer within IIB

Interventions

treatment group:Preoperative routine nursing, fasting except carbohydrate diet after 12 PM before surgery, oral carbohydrate (pivotally energy) 800ml at 20:00 PM before surgery, oral carbohydrate (piv
Routine operating room operation
Four hours after the operation, nalbuphine was given 0.2mg/Kg&#32
control group :Preoperative routine nursing, fasting except carbohydrate diet after 12 PM before surgery, oral carbohydrate (pivotally energy) 800ml at 20:00 PM before surgery, oral carbohydrate (pivo
Routine operation was performed in the operating room during the operation. Three days after&#3

Sponsors

SHENGJING HOSPITAL OF CHINA MEDICAL UNIVERSITY
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. Laparotomy for cervical cancer within IIB according to "Guidelines for Diagnosis and Treatment of Cervical Cancer (2021 Edition)"; 2. 18 years old = age = 65 years old; 3. No distant lymph node and blood metastases were found in imaging data; 4. Oral nutritional supplementation was possible; 5. Indications for laparotomy and anesthesia were met; 6. ASA grades I-III; 7. All selected participants agreed to participate in this study and signed.

Exclusion criteria

Exclusion criteria: 1. Laparoscopic surgery; 2. Severe malnutrition requiring supplemental nutrition through enteral and parenteral routes; 3. Chronic kidney disease, ischemic heart disease, or diabetes; 4. Refused to sign the informed consent; 5. Patients admitted to the ICU after surgery; 6. Has been enrolled in other RCT trials; 7. The patient himself or the legally authorized person is unwilling to participate in the trial; 8. The investigator judges that the patient is not suitable for inclusion (such as severe hypoalbuminemia; or potential disputes).

Design outcomes

Primary

MeasureTime frame
The Numeric Pain Rating Scale(NPRS);

Secondary

MeasureTime frame
sleep time;Gastrointestinal recovery;visual analogue scale(VAS) score for pain;postoperative complication;Adverse clinical outcome;Blood routine;hepatic and renal function;electrolyte;TNF-a;IL-1ß;IL-6;IL-10;C-reactive protein(CRP);Additional dose and frequency;

Countries

China

Contacts

Public ContactOuyang Ling
Ouyang1964@163.com+86 18940251964

Outcome results

None listed

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