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Clinical study on postoperative analgesia of costal cartilage harvest

Clinical study on postoperative analgesia of costal cartilage harvest

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100047028
Enrollment
Unknown
Registered
2021-06-07
Start date
2020-11-01
Completion date
Unknown
Last updated
2022-01-18

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

Conditions

Rhinoplasty with autologous costal cartilage

Interventions

Group A:multimodal cocktail intercostal injection
Group B:intercostal nerve block with ropivacaine
Group C:intercostal nerve block with ropivacaine + patient-controlled analgesia

Sponsors

Plastic Surgery Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Those with a treatment plan for costal cartilage harvest from one rib (the 6th or 7th) for rhinoplasty; 2. Patients over the age of 18 with intact cognitive function (no gender restriction); 3. BMI 16~35 Kg/m2; 4. Patients with American Society of Anesthesiologists (ASA) score I~III; 5. The patient signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. An allergy or intolerance to any medicines used in multimodal cocktail intercostal injection or PCA regimen (ropivacaine, parecoxib sodium, epinephrine, compound betamethasone or sufentanil); 2. Chronic analgesic drugs use; 3. Unable to perform Numrical Rating scale (NRS); 4. Local skin infection and bleeding at the anesthesia puncture site; 5. Patients deemed by surgeons or anesthesiologists not suitable for inclusion.

Design outcomes

Primary

MeasureTime frame
visual analogue scale (VAS);

Secondary

MeasureTime frame
rescue analgesic consumption;postoperative complications;

Countries

China

Contacts

Public ContactFan Fei

Plastic Surgery Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College

fanfei@psh.pumc.edu.cn+86 1088772072

Outcome results

None listed

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