Naldebain and Video-assisted Thoracoscopic Surgery (NCT04962152) | Clinical Trial Compass
UnknownPhase 4
Naldebain and Video-assisted Thoracoscopic Surgery
Taiwan60 participantsStarted 2021-07-07
Plain-language summary
To evaluate the postoperative analgesic effect of combined use of NaldebainĀ® and thoracic paravertebral block in thoracoscopic surgery
Who can participate
Age range20 Years ā 65 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* 1\) Subject's age: 20\~65 years old
* 2\) American Society of Anesthesiologists (ASA) Physical Status classification: I\~III
* 3\) Patients who need postoperative pain relief due to thoracoscopic surgery
Exclusion Criteria:
* 1\. The patient suffers from a communication disorder
* 2\. The patient has coagulopathy
* 3\. Sick with obvious heart, lung, liver or kidney disease
* 4\. The patient's body mass index is less than 18.5 or greater than 35
* 5\. Pregnant patients
* 6\. Patients who took opioids for more than three weeks before surgery
* 7\. Patients with contraindications to local anesthesia
* 8\. Patients with a history of chronic pain
* 9\. Patients with a history of drug allergy to Naldebain
What they're measuring
1
postoperative analgesic effect
Timeframe: During the first one hour in the recovery room, the pain intensity was evaluated every 15 minutes.
2
postoperative analgesic effect
Timeframe: the pain intensity was evaluated at 3 hours after surgery.
3
postoperative analgesic effect
Timeframe: the pain intensity was evaluated at 6 hours after surgery.
4
postoperative analgesic effect
Timeframe: the pain intensity was evaluated at 12 hours after surgery.
5
postoperative analgesic effect
Timeframe: the pain intensity was evaluated at 24 hours after surgery.
6
postoperative analgesic effect
Timeframe: the pain intensity was evaluated at 36 hours after surgery.
7
postoperative analgesic effect
Timeframe: the pain intensity was evaluated at 48 hours after surgery.
8
postoperative analgesic effect
Trial details
NCT IDNCT04962152
SponsorKaohsiung Medical University Chung-Ho Memorial Hospital