Skip to content

Methadone IV versus Paravertebral Catheter Block for analgesia in Video Assisted Thoracoscopic Surgery

Intravenous Methadone versus Paravertebral Catheter Block for analgesia in Video Assisted Thoracoscopic Surgery

Status
Not yet recruiting
Phases
Phase 3
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12624001346561
Acronym
MIVATS
Enrollment
90
Registered
2024-11-07
Start date
2024-12-01
Completion date
2025-12-01
Last updated
2024-11-11

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

Conditions

None listed

Brief summary

Video assisted thoracoscopic surgery (VATS) has become the standard of care for pulmonary lobectomy but the optimal perioperative analgesic regime remains unclear. Further, acute perioperative pain has been identified as one of the strongest predictors for the development of chronic pain after VATS which is seen in in over 30% of post VATS patients. Methadone has emerged as an alternative agent which provides prolonged analgesia lasting 24 to 48 hours; with the potential to reduce the requirement for short-acting opioids in the postoperative period An audit at Fiona Stanley Hospital also demonstrated that the current standard of care using paravertebral catheter block may not provide adequate pain control for patients after VATS lobectomy. Our study will explore whether IV methadone alone or a combination with paravertebral catheter block is an effective way of improving analgesic outcomes for patients after VATS lobectomy

Interventions

All participants will undergo a Video-Assisted Thoracoscopic Surgery (VATS) lobectomy to remove one or more segments of lung. The VATS lobectomy will be performed by a cardiothoracic surgeon and may take approximately 2-3 hours. This procedure may be performed in combination with other surgical procedures. Anaesthetic and procedural records will be used to monitor adherence to the treatment arms. Three treatment arms are to be used in this research project, but only two treatment arms include

All participants will undergo a Video-Assisted Thoracoscopic Surgery (VATS) lobectomy to remove one or more segments of lung. The VATS lobectomy will be performed by a cardiothoracic surgeon and may take approximately 2-3 hours. This procedure may be performed in combination with other surgical procedures. Anaesthetic and procedural records will be used to monitor adherence to the treatment arms. Three treatment arms are to be used in this research project, but only two treatment arms include the intervention (Arm 1 and 3). Arm 1: Intravenous Methadone on Induction of anaesthesia (IVMI): • 0.2mg/kg (max 20mg) Methadone administered intravenously on induction of General Anaesthesia (GA) as the sole opiate for case Arm 2: Standard Care • Paravertebral catheter block: Infusion of 0.2 % Ropivacaine via paravertebral catheter o Initial loading dose of 2-3mg/kg o intermittent mandatory bolus of between 0.25mg/kg every 4 hours • Fentanyl may additionally be administered intravenously with dosage determined by the anaesthetist according to patient factors – A maximum dose of 500mcg will be administered intraoperatively. Arm 3: Combination • 0.2mg/kg Methadone administered intravenously on induction of general anaesthesia • Paravertebral catheter block as for Standard of Care The paravertebral catheters will remain in situ with intermittent mandatory bolus of 0.2% Ropivacaine for the duration of the procedure and recovery until deemed no longer required by the treating team or Acute Pain Service (APS).

Sponsors

South Metropolitan Health Service
Lead SponsorGovernment body

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

• Undergoing a VATS lobectomy • Adult patients aged 18 – 80yo. • Able and willing to provide informed consent.

Exclusion criteria

• Paediatric patients aged <18, or patients aged >80yo. • Primary planned/unplanned open surgery. • Prior adverse reaction to methadone or local anaesthesia. • Chronic pain requiring gabapentinoids or opiates. • Current use of methadone or naltrexone for opioid use disorder. • Surgery lasting less than 1 hour. • Unable or unwilling to provide informed consent.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026