Naldebain and Video-assisted Thoracoscopic Surgery
Primary Purpose
Analgesia, Nausea and Vomiting, Postoperative, Itching
Status
Recruiting
Phase
Phase 4
Locations
Taiwan
Study Type
Interventional
Intervention
Nalbuphine Sebacate or Sesame oil (placebo)
Sponsored by
About this trial
This is an interventional treatment trial for Analgesia
Eligibility Criteria
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
Sites / Locations
- Department of Anesthesiology, Kaohsiung Medical University HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Group Naldebain
Group Placebo
Arm Description
ultrasound-guided intramuscular injection of Naldebain 150mg after the induction anesthesia immediately
ultrasound-guided intramuscular injection of sesame oil (placebo) 2mL after the induction anesthesia immediately
Outcomes
Primary Outcome Measures
postoperative analgesic effect
Use the visual analogue scale (VAS) score to assess the degree of pain after surgery
postoperative analgesic effect
Use the visual analogue scale (VAS) score to assess the degree of pain after surgery
postoperative analgesic effect
Use the visual analogue scale (VAS) score to assess the degree of pain after surgery
postoperative analgesic effect
Use the visual analogue scale (VAS) score to assess the degree of pain after surgery
postoperative analgesic effect
Use the visual analogue scale (VAS) score to assess the degree of pain after surgery
postoperative analgesic effect
Use the visual analogue scale (VAS) score to assess the degree of pain after surgery
postoperative analgesic effect
Use the visual analogue scale (VAS) score to assess the degree of pain after surgery
postoperative analgesic effect
Use the visual analogue scale (VAS) score to assess the degree of pain after surgery
Secondary Outcome Measures
Full Information
NCT ID
NCT04962152
First Posted
July 5, 2021
Last Updated
June 22, 2023
Sponsor
Kaohsiung Medical University Chung-Ho Memorial Hospital
1. Study Identification
Unique Protocol Identification Number
NCT04962152
Brief Title
Naldebain and Video-assisted Thoracoscopic Surgery
Official Title
To Explore the Effects of Naldebain Combined With Thoracic Paravertebral Block in Video-assisted Thoracoscopic Surgery.
Study Type
Interventional
2. Study Status
Record Verification Date
July 2022
Overall Recruitment Status
Recruiting
Study Start Date
July 7, 2021 (Actual)
Primary Completion Date
May 7, 2024 (Anticipated)
Study Completion Date
May 7, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Kaohsiung Medical University Chung-Ho Memorial Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
To evaluate the postoperative analgesic effect of combined use of Naldebain® and thoracic paravertebral block in thoracoscopic surgery
Detailed Description
Video-assisted thoracoscopic surgery (VATS) can be associated with stronger postoperative pain than is commonly believed. Pain control after thoracic surgery is important because increased acute pain has been shown to increase the incidence of chronic pain, and untreated pain may lead to increased morbidity. It is generally accepted to introduce multimodal analgesic strategies based on regional blockade, opioids and non-steroidal anti-inflammatory drugs.
Paravertebral block (PVB) involves the injection of local anesthetic into a wedge-shaped space lateral to the spinal nerves as they emerge from intervertebral foramina. It produces ipsilateral somatosensory and sympathetic nerve blockade effective for anesthesia as well as for management of pain of unilateral origin from the chest and abdomen. So far, thoracic paravertebral block (TPVB) is the most common technique used for patients undergoing VATS. TPVB may be useful after VATS because a single injection of local anesthesia may provide effective analgesia for the intense short-duration pain that patients experience.
Nalbuphine sebacate (Naldebain®) is a long-acting prodrug of nalbuphine developed for meeting the unmet medical need of long-acting analgesics. It is a synthetic opioid agonist-antagonist analgesic of the phenanthrene series. It is chemically related to both the widely used opioid antagonist, naloxone, and the potent opioid analgesic, oxymorphone. The currently proposed clinical use of nalbuphine sebacate is a single dose of Naldebain® administered intramuscularly approximately 24 h prior to the planned surgery for pain relief.
The purpose of this study is to determine the safety and efficacy of TPVB combined with a single dose of intramuscular Naldebain® administered preoperatively to patients scheduled to undergo VATS.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Analgesia, Nausea and Vomiting, Postoperative, Itching, Injection Site Reaction, Satisfaction, Patient
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Group Naldebain
Arm Type
Experimental
Arm Description
ultrasound-guided intramuscular injection of Naldebain 150mg after the induction anesthesia immediately
Arm Title
Group Placebo
Arm Type
Placebo Comparator
Arm Description
ultrasound-guided intramuscular injection of sesame oil (placebo) 2mL after the induction anesthesia immediately
Intervention Type
Drug
Intervention Name(s)
Nalbuphine Sebacate or Sesame oil (placebo)
Other Intervention Name(s)
Naldebain ER
Intervention Description
ultrasound-guided intramuscular injection after the induction of anesthesia immediately
Primary Outcome Measure Information:
Title
postoperative analgesic effect
Description
Use the visual analogue scale (VAS) score to assess the degree of pain after surgery
Time Frame
During the first one hour in the recovery room, the pain intensity was evaluated every 15 minutes.
Title
postoperative analgesic effect
Description
Use the visual analogue scale (VAS) score to assess the degree of pain after surgery
Time Frame
the pain intensity was evaluated at 3 hours after surgery.
Title
postoperative analgesic effect
Description
Use the visual analogue scale (VAS) score to assess the degree of pain after surgery
Time Frame
the pain intensity was evaluated at 6 hours after surgery.
Title
postoperative analgesic effect
Description
Use the visual analogue scale (VAS) score to assess the degree of pain after surgery
Time Frame
the pain intensity was evaluated at 12 hours after surgery.
Title
postoperative analgesic effect
Description
Use the visual analogue scale (VAS) score to assess the degree of pain after surgery
Time Frame
the pain intensity was evaluated at 24 hours after surgery.
Title
postoperative analgesic effect
Description
Use the visual analogue scale (VAS) score to assess the degree of pain after surgery
Time Frame
the pain intensity was evaluated at 36 hours after surgery.
Title
postoperative analgesic effect
Description
Use the visual analogue scale (VAS) score to assess the degree of pain after surgery
Time Frame
the pain intensity was evaluated at 48 hours after surgery.
Title
postoperative analgesic effect
Description
Use the visual analogue scale (VAS) score to assess the degree of pain after surgery
Time Frame
the pain intensity was evaluated at 72 hours after surgery.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hung-Te Hsu, MD, PhD
Phone
+88673121101
Ext
7033
Email
hdhsu1228@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Hung-Te Hsu, MD, PhD
Phone
+88673701260
Email
hdhsu1228@yahoo.com.tw
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hung-Te Hsu, MD, PhD
Organizational Affiliation
Department of anesthesiology, Kaohsiung Medical University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Anesthesiology, Kaohsiung Medical University Hospital
City
Kaohsiung City
ZIP/Postal Code
833
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hung-Te Hsu, MD, PhD
Phone
+88673121101
Ext
7033
Email
hdhsu1228@hotmail.com
12. IPD Sharing Statement
Learn more about this trial
Naldebain and Video-assisted Thoracoscopic Surgery
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