A Study Investigating Pain Following Single-port or Multi-port Video Assisted Thoracoscopic Surgery

Pain, Postoperative Clinical Trial

— SiMuPort  

Official title:

A Randomised Multi-centre Feasibility Study Investigating Post-operative Pain Following Single-port or Multi-port Video Assisted Thoracoscopic Surgical (VATS) Procedures

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT02556970
• Other study ID #: SU/2014/4744
• Status: Withdrawn
• Phase: N/A
• First received: September 4, 2015
• Last updated: November 14, 2016

Study information

• Verified date: November 2016
• Source: University Hospitals Bristol NHS Foundation Trust
• Contact: n/a
• Is FDA regulated: No
• Health authority: United Kingdom: Research Ethics Committee
• Study type: Interventional

Clinical Trial Summary

This study seeks to establish if thoracoscopic surgery performed through a single port or incision reduces early post-operative pain compared with conventional multiple port thoracoscopic surgery.

This initial pilot study is designed to establish whether a trial of the two techniques is acceptable to patients, clinically feasible and can be delivered in a reasonable timescale.

Description:

This is a patient- and assessor-blinded, multi-centre randomised trial with two groups (n=20 in each arm). Patients referred to Universities Hospital Bristol NHS Foundation Trust (n=20) and Liverpool Heart and Chest Hospital NHS Foundation Trust (n=20) requiring elective VATS lung surgery.

Patients will be identified and recruited by the thoracic surgeons in their surgical outpatient clinic. Participants will receive verbal and written information about the two different surgical techniques.

Consent will be sought by one of the surgical research nurses in the surgical outpatient clinic after the thoracic surgeon has recruited them. On the rare occasion that this is not possible, consent will occur in the pre-operative assessment clinic (POAC) at a later date. All patients are seen in POAC at least 1 week prior to surgery except in extreme circumstances. In POAC consent will also be sought by one of the surgical research nurses.

Participants will be given contact details for the study team should they have any questions between consent and surgery. They will be able to withdraw consent at any time prior to surgery.

All data will be entered into a Trust-based computer that is password protected. Subject names will be kept on a database and will be linked only with a study identification number for this research. There will be no patient identifiers. Only the research team will have access to this computer. Data will be stored in a locked office and maintained for a minimum of five years after the completion of the study.

Participants will be block randomised 1:1 in blocks of 10 between single port surgery and multiple port surgery. Randomisation will occur by computer generation in theatre after induction of anaesthesia using the website www.sealedenvelope.com.

The treatment arm will involve performance of the planned surgical procedure through a single incision in the chest wall, without rib spreading. The camera and instruments will be placed through this single incision. Use of a soft tissue retractor is permitted.

The control arm will undergo the operation through a standard 3-incision approach, again without rib spreading.

All patients will receive skin dressings matching those for the multi-port technique, irrespective of randomised allocation. Patients will be informed not to remove these dressings for the first 24 hours. Surgical and anaesthetic staff members will be informed not to communicate information about the treatment allocation to the patient or nursing staff. The patient and the nursing staff undertaking pain assessments will not be aware of group allocation for the first 24 hours. The research nurses collecting the data will also be blinded.

The anaesthetic and surgical team involved cannot practically be blinded but will not be involved in outcome data collection.

All patients will receive simple intra-operative analgesia in the form of 1g intravenous paracetamol and 75mg intravenous diclofenac unless the patient is over 70 or has abnormal renal function. Extra opioid analgesia will be given as intravenous fentanyl or morphine and this will be titrated by the anaesthetist. The amount given will be documented as part of the trial data.

At the end of the procedure, multiple level (target at least 4) intercostal blocks will be placed subpleurally under thoracoscopic visualisation. 2ml of 2.5mg/ml Chirocaine (Levobupivicaine hydrochloride) will be injected into each space.

Post-operative analgesia will compromise of 1g paracetamol four times a day for the first 3 days after surgery. Patient will receive IV morphine titrated to pain in recovery and oramorph when they return to the ward. If patient is in significant pain a morphine patient controlled analgesia (PCA) will be set up in recovery and for the first night after surgery (1mg bolus, lockout 5mins). This will normally be discontinued on the first morning after surgery.

The following data will be recorded for all patients enrolled in the study:

Pre-operatively:

• At consent, a baseline quality of life score will be recorded.

Intra-operatively:

The following times will be recorded on a sticker attached to the patient's anaesthetic chart:

• Time of induction of anaesthesia

• Time of knife to skin

• Time of skin closure

• Time of extubation

• Time arrived in recovery These times will be recorded by the research nurses allowing the total surgical time (induction to skin closure) and total operative time (knife to skin to skin closure) to be calculated.

Post-operative period (expected to be 36-48 hours post-surgery):

• Visual Analogue Scale (VAS) pain scores are routinely recorded by the recovery nurses and ward nurses every hour for the first 24 hours post operatively and subsequently every 4 hours until discharge. So assuming the time into recovery is time zero the investigators will collect a pain score at time zero and then every hour for the first 24 hours. The investigators will then collect a pain score every 4 hours until discharge.

• Patient satisfaction survey will be conducted on day 1 and day 2 post-op.

• Total morphine consumption prior to discharge will be recorded.

• Time of discharge.

• Length of time chest drain remains in situ.

• Volume of blood loss in chest drain in first 24 hours.

At 30 days:

• All patients will complete a telephone quality of life score.

• Serious adverse events recorded in first 30 days:

• Death

• Readmission to hospital

• Re-operation

• Admission to ICU

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. primary completion date: September 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Subjects will be recruited from patients requiring VATS for elective lung, lymph node or mediastinal biopsies or wedge resections of pulmonary nodules.

• Technically suitable for both single port or multiport approaches in the opinion of the recruiting surgeon.

• ASA 1,2 or 3.

Exclusion Criteria:

• Pregnancy or breastfeeding.

• Patient refusal.

• Emergency surgery.

• Patient unable to provide consent or complete the follow up.

• Patients who attend a chronic pain clinic on high doses of opiate drugs.

• History of Anaphylaxis/allergy to local anaesthetic.

• Lobectomy patients.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Pain, Postoperative

Intervention

Procedure:
• Single port VATS
Performing video-assisted thorascopic surgery through a single port

Drug:
• Paracetamol
1g intraoperatively
• Diclofenac
75mg intraoperatively

Device:
• Camera (5mm diameter 30 degree videothoracoscope)

• Forceps grasper

Drug:
• 0.25% Levobupivicaine intercostal nerve block
Multi-level intercostal blocks will be placed subpleurally under thorascopic visualisation.

Locations

Country	Name	City	State
n/a

Sponsors (2)

Lead Sponsor	Collaborator
University Hospitals Bristol NHS Foundation Trust	David Telling Charitable Trust

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Ability to randomise 40 patients into trial		3 months	No
Secondary	Median postoperative Visual Analogue Scale (VAS) pain score	VAS pain score; 0 = no pain, 10 = worst pain participant could imagine	Before discharge (24-48 hours)	No
Secondary	Maximum post operative Visual Analogue Scale (VAS) pain score	VAS pain score; 0 = no pain, 10 = worst pain participant could imagine	Before discharge (24-48 hours)	No
Secondary	Mean Visual Analogue Scale (VAS) pain score at 1 hour	VAS pain score; 0 = no pain, 10 = worst pain participant could imagine	1 hour after surgery	No
Secondary	Mean Visual Analogue Scale (VAS) pain score at 24 hours	VAS pain score; 0 = no pain, 10 = worst pain participant could imagine	At 24 hours after surgery	No
Secondary	Crossover after randomisation	Proportion of the trial (single port) arm converted to multiple port thoracoscopic or open approaches after randomisation	During surgery (normal surgical time is approximately 1 hour)	No
Secondary	Total post-operative morphine consumption (mg)	Total morphine dose in milligrams	In the first 24 hours post-surgery	No
Secondary	Mortality		30 days post-surgery	No
Secondary	Unexpected ICU admission		After surgery and before discharge (expected to be with in 48 hours)	No
Secondary	Hospital readmission rate	Readmission for any complication of the thoracic surgery.	Within 30 days of surgery	No
Secondary	Surgical site infection	Diagnosed infection in or around the surgical incisions.	Within 30 days of surgery	No
Secondary	Change in Quality of Life score		Performed pre-operatively and at 30 days after surgery	No