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Comparing the postoperative pain in children after pectus excavatum surgery between intercostal nerve block and patient-controlled analgesia

Comparing the postoperative pain in children after pectus excavatum surgery between intercostal nerve block and patient-controlled analgesia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018040
Enrollment
Unknown
Registered
2018-08-28
Start date
2018-09-01
Completion date
Unknown
Last updated
2018-09-03

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

Conditions

pectus excavatum in children

Interventions

Group 1:ultrasound-guided intercostal nerve block
Group 2:patient-controlled analgesia

Sponsors

Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) The volunteers sign the informed consent form voluntarily; 2)The patients with pectus excavatum accept Nuss surgery, aged 10-16 years; 3) ASA = II; 4) The volunteers can follow the plan of test and visit; 5) The volunteers, with normal coagulation function, without renal insufficiency, can objectively describe symptoms and cooperate actively; 6) Without local anesthetic allergy; 7) Without drug abuse or drug addiction; 8) no drug testing (including this trial drug) was conducted within 3 months before the test.

Exclusion criteria

Exclusion criteria: 1) Those who do not meet the inclusion criteria; 2) Requiring additional surgeries; 3) Analgesic drugs (including opioids, paracetamol or non-steroidal anti-inflammatory drugs) were used 24 hours before operation; 4) Patients with coagulation disorders; 5) Local anesthetic allergens; 6) History of renal insufficiency; 7) Inability to understand the use of patient controlled analgesia (PCA) or parents' rejection of intercostal nerve block; 8) History of drug abuse or drug addiction; 9) Patients who participated in the drug trial within 3 months prior to the trial (including the trial drug); 10) A sponsor or researcher who directly participates in the trial or their family members.

Design outcomes

Primary

MeasureTime frame
visual analogue scale score;

Secondary

MeasureTime frame
Consumption of opiates;Anxiety;Depression;Quality of life;sleep quality;

Countries

China

Contacts

Public ContactSai'e Shen

Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine

saie1971@sina.com+86 13801877258

Outcome results

None listed

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