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Effects of different anesthesia methods on postoperative recovery and prognosis of patients with colorectal tumors

Effects of total intravenous or inhalation anesthesia combined with intravenous infusion of lidocaine on postoperative plasma NETosis and angiogenesis markers in colorectal cancer patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100053586
Enrollment
Unknown
Registered
2021-11-24
Start date
2022-01-05
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

colorectal cancer

Interventions

Group 1:Intravenous anesthesia
Group 2:Intravenous anesthesia + lidocaine
Group 3:Ihalation anesthesia
Group 4:Inhalation anesthesia + lidocaine

Sponsors

Shanghai Changhai Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Preoperative diagnosis of colorectal cancer, including: left colon tumor, right colon tumor, transverse colon tumor, sigmoid colon tumor and rectal cancer, TNM clinical stage: stage II, patients with laparoscopic radical colorectal resection ; 2. ASA grade I, II or III; Aged 18-70 years; 3. During the preoperative screening and evaluation, the principal investigator and the assisting investigators, the patients can understand and comply with the research protocol, can communicate, and agree to sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Distant metastasis of colorectal tumor; 2. Preoperative neoadjuvant chemotherapy or radiotherapy; 3. Pregnant patients; 4. Hypersensitivity to lidocaine, ropivacaine, sufentanil, rocuronium bromide and other related anesthetics; 5. Long-term use of beta-blockers in the past; 6. Patients with chronic inflammatory disease or autoimmune disease before surgery, or previous long-term treatment with glucocorticoids or other immunosuppressive agents; 7. Preoperative coagulation dysfunction; 8. Preoperatively accompanied by severe heart disease (NYHA cardiac function class>3), severe renal insufficiency (serum creatinine>1.8mg/dL (159.1µmol/L) or receiving renal function replacement therapy), severe hepatic insufficiency (modified Child-Pugh class C); 9. Acute infection is not well controlled before surgery; with diabetes, preoperative blood sugar control is poor (fasting blood sugar control exceeds the range of 3.9-13.8mmol/L); 10. A history of drug abuse such as opioids; 11. Mental illness or cognitive dysfunction, inability to cooperate and poor compliance; 12. Patients with other contraindications to anesthesia or surgery.

Design outcomes

Primary

MeasureTime frame
Plasma NETosis-specific markers (MPO and H3Cit);Tumor progression and metastasis related markers (VEGF-A, MMP-3, MMP-9);

Secondary

MeasureTime frame
Incidence of moderate to severe pain during activity 24 hours after surgery (definition: activity: when taking 3 deep breaths or 1 coughing; moderate to severe pain: NRS score >= 4);Incidence of adverse reactions 24 hours after surgery (such as nausea, vomiting, respiratory depression (respiratory rate less than 8 breaths/min), incidence of constipation);Incidence of moderate to severe pain at rest 24 hours after surgery;24h postoperative rehabilitation quality score (15-item Quality of Rehabilitation Rating Scale (QoR-15)), incidence of respiratory complications during postoperative hospitalization, incidence of chronic pain at 3 months, 6 months and 1 year after surgery, Hospitalization days, hospitalization expenses, etc.;

Countries

China

Contacts

Public ContactBo Lulong

Shanghai Changhai Hospital

nbastars@126.com+86 13817283189

Outcome results

None listed

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