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Multimodal Analgesia Decreases Pain Following VATS: A Prospective, Non-randomized Clinical Trial

Multimodal Analgesia Decreases Pain Following VATS: A Prospective, Non-randomized Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000030144
Enrollment
Unknown
Registered
2020-02-24
Start date
2017-09-01
Completion date
Unknown
Last updated
2020-02-25

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

Conditions

Thoracic disease

Interventions

Sponsors

Taizhou Enze Medical Center (Group) Enze Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Of the American society of anesthesiologists (ASA) Physical Status Classification Score from I to III; (2) Aged from 18 to 80 years; (3) Undergoing video-assisted thoracic surgery (VATS) for lung, mediastinal or esophageal diseases; (4) Operation time is expected to be within 1 ~ 6 h; (5) The number of operation ports from 1 to 5.

Exclusion criteria

Exclusion criteria: (1) Patients with chronic obstructive pulmonary disease (COPD), type 2 diabetes or chronic pain before surgery; (2) Patients who received immunosuppressive drugs before surgery; (3) Patients who do not cooperate due to mental disorder or other reasons; (4) Patients who participated in other drug clinical studies in the last 3 months; (5) Patients with hemoglobin (Hb)<80 g/L.

Design outcomes

Primary

MeasureTime frame
Numeric Rating Scale, NRS;

Secondary

MeasureTime frame
Side Effects;

Contacts

Public ContactMin Kong

Taizhou Enze Medical Center (Group) Enze Hospital

kongmin007@aliyun.com+86 13586115975

Outcome results

None listed

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