NCT04829409

Brief Summary

Ultrasound-guided mid-point transverse process to pleura block, erector spinae plane block and paravertebral block are three different methods of nerve block, used for relieving postoperative pain in thoracic anesthesia. This study is to compare them on block effects, postoperative pain and analgesic consumption in video-assisted thoracic surgery.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
90

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Apr 2021

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 30, 2021

Completed
3 days until next milestone

First Posted

Study publicly available on registry

April 2, 2021

Completed
3 days until next milestone

Study Start

First participant enrolled

April 5, 2021

Completed
1.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2022

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2022

Completed
Last Updated

April 14, 2022

Status Verified

April 1, 2022

Enrollment Period

1.5 years

First QC Date

March 30, 2021

Last Update Submit

April 13, 2022

Conditions

Keywords

ultrasound-guided nerve blockpostoperative pain

Outcome Measures

Primary Outcomes (1)

  • postoperative morphine consumption

    The dose is according to the record from PCA pump

    postoperative 24 hours

Secondary Outcomes (2)

  • Pain score at rest

    at 0, 8, 24 hour after surgery

  • Pain score while coughing

    at 0, 8, 24 hour after surgery

Other Outcomes (2)

  • block level

    20 minutes after block

  • intraoperative analgesic comsumption

    intraoperative, from induction to emergence from anesthesia

Study Arms (3)

paravertebral block

ACTIVE COMPARATOR

Patients receive ultrasound-guided paravertebral block

Procedure: Paravertebral block

ESP block

ACTIVE COMPARATOR

Patients receive ultrasound-guided erector spinae plane (ESP) block

Procedure: ESP block

MTP block

EXPERIMENTAL

Patients receive ultrasound-guided mid-point transverse process to pleura (MTP) block

Procedure: MTP block

Interventions

Patients receive ultrasound-guided paravertebral block

paravertebral block
ESP blockPROCEDURE

Patients receive ultrasound-guided erector spinae plane (ESP) block

ESP block
MTP blockPROCEDURE

Patients receive ultrasound-guided mid-point transverse process to pleura (MTP) block

MTP block

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • selective lobetomy under VATS
  • ASA classfication 1-3

You may not qualify if:

  • history of thoracic surgery
  • double lateral VATS
  • allergy to local anesthetics
  • coagulation disorders
  • severe heart diseases, hepatic or renal insufficiency
  • a history of chronic pain or chronic opioid use
  • psychiatric disease or uncooperative
  • BMI\>28 kg/m2
  • VATS transfered to open thoractomy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Tongji Hospital, Huazhong University of Science and Technology

Wuhan, Hubei, 430030, China

RECRUITING

MeSH Terms

Conditions

Acute PainPain, Postoperative

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsPostoperative ComplicationsPathologic Processes

Study Officials

  • Ailin Luo, MD,PhD

    Tongji Hospital

    STUDY CHAIR

Central Study Contacts

Wenlong Yao, MD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

March 30, 2021

First Posted

April 2, 2021

Study Start

April 5, 2021

Primary Completion

October 1, 2022

Study Completion

December 1, 2022

Last Updated

April 14, 2022

Record last verified: 2022-04

Locations