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A multicenter randomized study of intrathecal preemptive analgesia in improving chronic pain after pulmonary surgery

Effects of intrathecal injection of opioids and/or local anesthetics on acute and chronic pain and postoperative rehabilitation after pulmonary surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059106
Enrollment
Unknown
Registered
2022-04-25
Start date
2022-04-26
Completion date
Unknown
Last updated
2024-02-11

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

Conditions

Lung cancer and lung nodules

Interventions

Group QB:Intrathecal morphine and bupivacaine
Group Q:Intrathecal morphine
Group B:Intrathecal bupivacaine
Group C:None

Sponsors

Affiliated Hospital of Yangzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Elective thoracoscopic lobectomy was performed in patients aged 18-65 years, no gender limit; 2. ASA Grade I-II, BMI 18-30 kg/m^2; 3. Plan to stay in hospital >= 48 hours after surgery; 4. Be aware of and volunteer for the study.

Exclusion criteria

Exclusion criteria: 1. Patients with severe cardiac, liver and renal dysfunction before surgery; 2. Long-term users of analgesic and sedative drugs and alcoholics; 3. There are infected people at the puncture site; 4. Patients with severe cerebrovascular disease, Alzheimer's disease, epilepsy, Parkinson's disease and other neuropsychiatric diseases; 5. Previous history of intracranial surgery or craniocerebral injury; 6. Severely impaired in vision, hearing, speech, or unable to communicate for other reasons; 7. Those who are allergic to or contraindicated with morphine, local anesthetics and non-steroidal anti-inflammatory drugs (NSAID); 8. Patients with coagulation dysfunction; 9. Patients with bronchial asthma, hypothyroidism, prostatic hypertrophy and dysuria.

Design outcomes

Primary

MeasureTime frame
acute pain score;chronic pain score;postoperative recovery index;the incidence of adverse reactions;

Secondary

MeasureTime frame
total opioids;

Countries

China

Contacts

Public ContactZhang Jianyou

Affiliated Hospital of Yangzhou University

zhangjianyou@yzu.edu.cn+86 13815813811

Outcome results

None listed

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