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Minimally Invasive or Open Surgery for Lung Cancer: Pain, Quality of Life and Economy.

18 Years
Open (Enrolling)
Nonsmall Cell Lung Cancer Cellular Diagnosis

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Trial Information

Minimally Invasive or Open Surgery for Lung Cancer: Pain, Quality of Life and Economy.

Is minimally invasive surgery for non small cell lung cancer better than traditional open

Surgical resection remains the best treatment for non small cell lung carcinoma (NSCLC),but
unfortunately many patients suffer major postoperative morbidity - pain being the most
frequent. It is assumed that newer minimally invasive surgical techniques (Video Assisted
Thoracoscopic Surgery - VATS) reduces postoperative morbidity but there is no level 1
evidence available in the literature. This prompted us to perform the present ongoing study,
which is the first of its kind in the world.

The investigators compare VATS with traditional open surgery for early stage lung cancer in
a clinical randomized double blinded trial. Our aims are to evaluate differences in
postoperative pain, life quality, and health economical aspects. The results of this trial
could influence future surgical decisionmaking internationally on the surgical treatment for
lung cancer.

Likewise, in patients with larger tumours of the lung, which are not suitable for minimally
invasive surgery, different techniques are available. The most widely used techniques are
the posterolateral thoracotomy and the anterolateral thoracotomy. So far no randomized
controlled trail has shown which of these techniques to be superior. This has led us to also
randomize between anterolateral and the posterolateral thoracotomy (muscle sparing). The
same endpoints are used.

Pain following lung surgery has been a much discussed topic for a long time in the field of
thoracic surgery. Depending on the reference, up to 50% of patients develop chronic pain
after open lung surgery. Therefore, different surgical approaches have been developed
including anterior, lateral or posterior thoracotomy with or without sparing the chest wall
muscles. The intercostal nerve is also of concern because of trauma from the rib retractor
which is believed to be a cause of both acute and chronic pain. Other concerns are the
amount of divided tissue, extend of rib displacement by the rib retractor, type of
analgesics, administration form of analgesics, and administration time of the analgesics and
it is generally accepted that pain in lung cancer patients is multifactorial.

VATS was introduced in an attempt to reduce the surgical trauma with less tissue damage,
avoidance of the rib retraction and the consequently intercostal nerve injury, but never the
less several patients develop chronic pain after lung surgery by VATS.

Information on quality of life and health economical aspects following surgery for lung
cancer are scarce. No randomized controlled trial has been published. Very little is known
if lung cancer patients regain their workability and if so to what extent following surgery.

Likewise, it is not known if VATS is more costly than open procedures, as the opponents say,
or if increased expenses during hospitalization are saved by earlier return to work.

Inclusion is well on the way. Other centers have shown interest in participating in the
project. Follow up has been completed for a number of patients, and the results at beginning
to mount up, waiting to be analyzed.

End points

1. Postoperative pain evaluated using the VAS-score and the need for prescription
analgetics 2, 4, 8, 12, 26 and 52 weeks after surgery.

2. Health related life quality and workability and -efficiency in the same period, using
three different questionnaires: two concerning life quality (EORTC-QLQC-30 and EQ5D)
and one concerning workability (WPAI).

3. Health economical aspect such as application for pension, visits to general
practitioner, readmitted to hospital, number of days away from work due to
postoperative morbidity, etc.

All gathered from different databases managed by "Danmarks Statistik" here among the
"Landspatientregistret(LPR)", "Sygesikringsstatistikregistret" ,and

250 patients admitted to the department of cardiothoracic surgery, Odense University
Hospital, for elective surgery for lung cancer will be included in each study.


This research project has three sub studies: Two randomized controlled and double blinded
clinical trials, and one registry study. One clinical trial randomizes patients with small
peripheral lung cancer between VATS (Video Assisted Thoracoscopic Surgery) and standard open
anterolateral thoracotomy. The second clinical trial randomizes between anterolateral and
posterolateral open thoracotomy in patients not eligible for VATS. The registry sub study
monitors patients use of analgetics during the first 12 months
(lægemiddelstatestik-registret), their use of other health services, and return to work.

All patients will be operated in general anaesthesia with a double lumen tracheal tube and
an epidural catheter. The epidural catheter will be removed when all chest tubes has been
removed, but no later than postoperative day 4.

As a standard all patients will be given paracetamol and NSAID in standard doses, and if
needed opioids (oxycontin/oxynorm) can be added.

All surgical techniques will be performed as routine operations.

Three different surgical techniques will be used.

1. The VATS approach: one camera port and three assistance ports one of which is enlarged
to 5 cm. and rib retractors are never used.

2. Anterolateral thoracotomy: The incision is made from the posterior axillary fold
following the linea inframammary to a point below the papilla.

3. Posterolateral thoracotomy. The incision is made from the anterior axillary fold
backwards towards the inferior angle of the scapula, without dividing the dorsal
latissimus muscle.

In both clinical trials postoperative pain is evaluated by a visual analog scale (VAS). Pain
is measured during rest and during coughing. Measurements are done preoperatively and 6
times daily during their hospital stay. After discharge measurements are recorded after 2,
4, 8, 12, 26, and 52 weeks by mail questionnaire.

Both patients and the staff doing general rounds postoperatively will be blinded. In the
operating room a dressing will be placed so that it covers the entire hemithorax whereby the
incision is hidden. This is done identically regardless of surgical technique. This dressing
is left in place until discharge. If changing of the dressing is needed, either the
project-nurse or a nurse for another team will assist.

The surgical note is kept in a sealed envelope, which is always placed in the patients chart
and can be opened in case of emergency. The chart will only include information about which
lobe was resected, no details on the surgical access, but this information is added when the
patient is discharged.

The surgeon who has performed the operation will be allowed to check up on their own
patients, and to be consulted by the other doctors doing rounds, but they are not allowed to
influence on decision-making regarding pain relief or discharge, during the postoperative


This project is a combination of a ph.d-study and a residency/fellowship in cardiothoracic
surgery because this allows for a longer inclusion period. The timeline is divided into
three research periods and three clinical periods.

This research project has already been accepted as a ph.d.-project at the University of
Southern Denmark, and approved by the local ethical board.

Inclusion Criteria:

- Eligible for surgery for lunge cancer.

- Elective surgery (surgery planed > 2 days)

- Accepts randomization

- Age 18 or above.

Exclusion Criteria:

- Previous thoracic surgery

- Planned segment resection or pneumonectomy.

- Any type of chronic pain, requiring daily use of analgetics

- pregnant

- Breast feeding

- T3, T4 tumors or cerebral tumors.

- contraindications to NSAID

- Chemo- and/or radiotherapy in connection to present admission.

- Major surgery planned in connection to this admission.

Type of Study:


Study Design:

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Treatment

Outcome Measure:

Postoperative pain

Outcome Description:

Aim is to asses the development of acute and chronic pain after lobectomy.

Outcome Time Frame:

12 months

Safety Issue:


Principal Investigator

Peter B Licht, Professor

Investigator Role:

Study Director

Investigator Affiliation:

Dept. Cardithoracic and Vascular Surgery


Denmark: Danish Dataprotection Agency

Study ID:




Start Date:

September 2008

Completion Date:

August 2014

Related Keywords:

  • Nonsmall Cell Lung Cancer Cellular Diagnosis
  • Lung cancer
  • Pain
  • Quality of life
  • Economy
  • Carcinoma, Non-Small-Cell Lung
  • Lung Neoplasms