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Multimodal Analgesic Management of Naborphine Combined With Opioid Free Anesthesia in OSA Patients Undergoing Bariatric Surgery

Multimodal Analgesic Management of Naborphine Combined With Opioid Free Under General Anesthesia in OSA Patients Undergoing Weight Loss Surgery Under the Concept of ERAS: a Prospective, Randomized, Parallel Controlled Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05386979
Enrollment
48
Registered
2022-05-24
Start date
2022-05-15
Completion date
2023-10-31
Last updated
2022-05-24

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

Conditions

Analgesics,Opioid, Bariatric Surgery

Keywords

Opioid free anesthesia, Bariatric Surgery, ERAS

Brief summary

Comparative study to explore the effect of opioid free anesthesia technology in perioperative analgesia management, clarify the effect of naborphine instead of opioids on perioperative analgesia management in morbid obesity patients with moderate and severe OSA, reduce related adverse events, and explore the latest clinical anesthetic drugs.

Detailed description

1. The concept of enhanced recovery after surgery (ERAS) has been applied in the perioperative period of many operations. Reducing the dosage of opioids is an important part of the concept of ERAS. 2. Opioid free anesthesia technology has been recognized in reducing nausea and vomiting, but whether it can meet the perioperative analgesic needs of patients undergoing bariatric surgery and obtain more clinical benefits still has no research supportment. 3. This study is expected to clarify the clinical effect of opioid free anesthesia technology in perioperative analgesia management of morbid obesity patients with moderate and severe OSA, reduce adverse events, and explore the latest clinical anesthesia scheme.

Interventions

PROCEDUREOpioid free anesthesia technology

We have adopted a variety of methods to replace the use of opioids in the process of balanced anesthesia.

Sponsors

Qianfoshan Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

1. ASA grade I \ III; 2. Age from 18 - 65 years old; 3. BMI ≥ 35kg / m2 in patients with OSA to undergo bariatric surgery; (4 provide written informed consent for participation.

Exclusion criteria

1. Age \< 18 years or age \>65 years old; 2. Pregnancy test was positive; 3. Patients with a history of drug abuse or dependence on opioids; 4. Patients with chronic pain or severe heart, lung, liver or nervous system diseases

Design outcomes

Primary

MeasureTime frameDescription
postoperative NRS scoreScore from the end of the operation and follow-up at the time point specified in the scoring form for a total of 27 hours.A subjective psychometric response scale used to measure distinct behavioral or physiological phenomena based on linear numerical gradient or yes/no alternatives. The Numeric Pain Scale (NRS) pain numerical score(0-10 score, 0: no pain, 10: worst imaginable pain). A pain measurement list about quiet NRS score and cough NRS score at different postoperative time will be used.

Secondary

MeasureTime frameDescription
Hemodynamic fluctuationFrom the beginning of the general anesthesia induction to the time leaving PACU, it takes about 4 hours.Hemodynamic fluctuation during perioperative period. The levels of SBP in mmHg, DBP in mmHg, MAP in mmHg and HR in times/minute in basic(T0), after induction(T1), preoperative(T2) and after establishing pneumoperitoneum(T3) 1h after the pneumoperitoneum(T4) and Immediately after operation(T5), Before(T6) and after(T7) extubation were recorded.
Ramsay scaleScore from the end of the operation and follow-up at the time point specified in the scoring form for a total of 27 hours.Ramsay scale is the most widely used sedation scoring standard in clinic, which is simple and practical. This scale has multiple advantages: it is reproducible, easily executed and has good applicability. This has made the scale the most widely used to assess level of sedation for procedures in pediatrics. It is divided into six levels(1-6): 1 shows patient is anxious and agitated or restless, or both; 2 shows patient is co-operative, oriented, and tranquil; 3 shows patient responds to commands only; 4 shows patient exhibits brisk response to light tactile stimuli or loudauditory stimulus; 5 shows patient exhibits sluggish response to light tactile stimuli or loud auditory stimulus; 6 shows patient exhibits no response.
recovery timeIt will take up to 1 hour or 2 hours.From the time when the patient entered PACU to the time when the participant meets the standard of leaving the PACU.
The levels of C-reactive protein (CRP)It takes about 24 hours.We will collect the participant's blood at the time before surgery(T0), after surgery(T1), and 24h after surgery(T2) to obtain the levels of C-reactive protein (mg/L).
The levels of cortisol (COR).It takes about 24 hours.We will collect the participant's blood at the time before surgery(T0), after surgery(T1), and 24h after surgery(T2) to obtain the levels of cortisol (nmol/L).
Dosage of remedial analgesics postoperativelyIt takes about 24 hours.If the participant still feels severe pain after operation and needs additional analgesic drugs for treatment, we will record the type and dose of drugs used by the patient.
The levels of interleukin-6 (IL-6).It takes about 24 hours.We will collect the participant's blood at the time before surgery(T0), after surgery(T1), and 24h after surgery(T2) to obtain the levels of IL-6 (pg/mL).
Scores of 15-item Quality of Recovery (QoR-15) scale 24 hours postoperatively of participants.One day after the surgery.The QoR-15 scale is a validated tool to assess the quality of postoperative recovery (QoR) from 0 to 150. The QoR was classified as excellent (QoR-15 \> 135), good (122 ≤ QoR-15 ≤ 135), moderate (90 ≤ QoR-15 ≤ 121) or poor (QoR-15 \< 90).
Rate of postoperative nausea and vomitingIt takes about 24 hours.Postoperative nausea and vomiting will be recorded if it happens.
Acceptability of participants with laryngeal mask 24 hours after surgery.One day after the surgery.One day after surgery, we will record the acceptability of laryngeal mask and the degree of postoperative pharyngeal pain of the participants. Acceptability of participants with laryngeal mask will be assessed by whether the participant was willing to receive laryngeal mask anesthesia again. Pharyngeal pain can be evaluated using the Numeric Pain Scale (NRS) pain numerical score. A subjective psychometric response scale used to measure distinct behavioral or physiological phenomena based on linear numerical gradient or yes/no alternatives. The Numeric Pain Scale (NRS) pain numerical score(0-10 score, 0: no pain, 10: worst imaginable pain).
The levels of blood glucose (BG)It takes about 24 hours.We will collect the participant's blood at the time before surgery(T0), after surgery(T1), and 24h after surgery(T2) to obtain the levels of blood glucose (mmol/L).

Countries

China

Contacts

Primary ContactYongtao Sun, doctor
sunyongtao1979@163.com18660795201

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026