Botulinum Toxin A as Treatment for Chronic Postsurgical Pain Following Lung Cancer Surgery

Chronic Pain Clinical Trial

Official title:

Botulinum Toxin A as Treatment for Chronic Postsurgical Pain Following Lung Cancer Surgery: a Randomized Controlled Pilot Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT04585620
• Other study ID #: 74719
• Status: Not yet recruiting
• Phase: Phase 1/Phase 2
• Start date: September 1, 2022
• Est. completion date: January 31, 2024

Study information

• Verified date: November 2021
• Source: Aalborg University Hospital
• Contact: Allan V Danielsen, MD
• Phone: +45 29720229
• Email: a.danielsen[@]rn.dk
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Chronic postsurgical pain following lung cancer surgery is common with and 20-60 % develop chronic pain which persists more than six months after surgery. Causes and health impact of this pain have been comprehensively studied. Current treatment consists of combination of pain medication, physiotherapy and psychological therapy. Botulinum Toxin A (BTX-A) has shown promising effects in a variety of chronic postsurgical pain syndromes. The use of BTX-A in lung cancer patients has only been presented in few case reports. No randomized controlled trials (RCT) have been executed to date. Study objectives: Determine recruitment potential among cured lung cancer patients with chronic postsurgical pain for an RCT and if the method of BTX-A administration is feasible and acceptable. Further more, this study will contribute to the stage testing of the hypothesis that chronic pain following thoracic surgery can be treated with BTX-A. Methods: Recruitment of test subjects: Participiants are recruited among former lung cancer patients with chronic postsurgical pain, who have undergone radical treatment for lung cancer at the Department of Cardiothoracic Surgery, Aalborg University Hospital. Potential test subjects are invited by mail / e-mail. Randomization and blinding: Participants are randomized to receive a single series of subcutaneous injections with either Onabotulinum Toxin A (active agent) or inactive normal saline (Placebo) at the former operation site. Neither participant nor investigator will know which treatment is given until the end of the trial. Data collection: Data is collected by questionnaires delivered and answered by mail or digitally. Data on the possible effects and possible adverse reactions are collected at multiple times until three months after treatment.

Description:

Chronic postsurgical pain (CPP) following lung cancer surgery is common with an observed prevalence of 20-60 %. Causes and health impact have been comprehensively studied. Current treatment consists of combination of pain medication, physiotherapy and psychological therapy. Botulinum Toxin A (BTX-A) has shown promising effects in a variety of chronic postsurgical pain syndromes. The use of BTX-A in lung cancer patients has only been presented in few case reports. No randomized clinical controlled trials (RCT) has been executed to date. Study objectives: Primary: Determine recruitment potential among cured lung cancer patients with CPP for an RCT and if the method of BTX-A administration is feasible and acceptable to the test subjects. Secondary: Early stage testing of the hypothesis that CPP following thoracic surgery can be treated with this novel method. Methods: Recruitment of test subjects: Test subjects are recruited among former lung cancer patients with chronic postsurgical pain, who have undergone radical treatment for lung cancer at the Department of Cardiothoracic Surgery, Aalborg University Hospital. Potential test subjects are invited by mail / e-mail. Randomization and blinding: Test subjects are randomized to receive a series of injections with either Onabotulinum Toxin A (active agent) or inactive normal saline (Placebo). Neither test subject nor investigator will know which treatment is given until the end of the trial. Experimental treatment: The investigator examines the skin area of the test subject at the operation site and performs a sensory examination with pin prick and sensory brush. The area is located and marked and divided into quadrants of one square centimeter. An area of maximum 40 square centimeters is marked. At a single treatment session, test subjects receives either active agent or placebo through a series of subcutaneous injections. One injection is given in each marked quadrant of the treatment area. The maximal number of injections is 40. Follow-up: After the treatment, test subjects report pain symptoms and intensity, use of pain medication and occurrence of adverse events weekly. After 30 and 90 days after treatment more comprehensive and additional data is collected concerning neuropathic symptoms, activities of daily life, general health and level of function. Data collection Data is collected by questionnaires delivered to test subjects by mail or digitally. Endpoints: Primary: 1. Recruitment of 30 test subjects. 2. Half of the first half of included test subject must complete the treatment. 3. Half of test subjects in total mus complete the treatment. Secondary: 1. Pain at rest, coughing and when active Numerical rating score (NRS) for presence of pain before and after treatment and course of pain symptoms. 2. General Health Short form 36 Health Survey on physical, social and mental level of function on a score from 0 to 100. 3. Neuropathic Pain Symptoms Inventory (NPSI) NRS 4. Activities of daily life Impact and intensity of pain categorically in 16 situations of daily life. 5. Patient's Global Impression of Change (PGIC) Rating of global change perceived by the test subject from "More Worse" to "Much better" and a scale from 0 to 10.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 30
• Est. completion date: January 31, 2024
• Est. primary completion date: December 31, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Patients of 18 years of age or above.

2. Patients who have undergone pulmonary surgery because of suspicion or confirmed pulmonary malignancies.

3. Patients who are radically treated for pulmonary malignancy

4. Patients who suffers from chronic pain or unpleasant sensation at the site of scar at least six months after surgery with fully healed surgical wounds.

Exclusion Criteria:

1. Patients who cannot understand oral and written information.

2. Patients who were not radically operated.

3. Patients with other concomitant or other active cancer diseases.

4. Patients with chronic pain in the chest wall prior to surgery.

5. Pregnant women or women planning to get pregnant in the study period.

6. Patients with autoimmune neuromuscular diseases, sclerosis, peripheral neuromuscular disturbances and general muscle weakness or atrophy.

7. Patients with intolerance or allergy to BOTOX®.

8. Patients who are at present treated with BTX-A or similar neuromuscular blocking drug or have received such in the past year.

Related Conditions & MeSH terms

• Chronic Pain
• Neuralgia
• Pain, Neuropathic
• Pain, Postoperative
• Post-thoracotomy Pain Syndrome

Intervention

Drug:
• Onabotulinum Toxin A
Series of subcutaneous injections
• Normal saline
Series of subcutaneous injections

Locations

Country	Name	City	State
Denmark	Dept. of Cardiothoracic Surgery, Aalborg University Hospital	Aalborg

Sponsors (1)

Lead Sponsor	Collaborator
Allan Vestergaard Danielsen, MD

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Incidence of treatment procedure disruption for the first half of test subjects	Half of the first half of included test subject must complete the treatment.	Through study inclusion period of 12 months
Primary	Rate of recruitment	Recruitment of 30 test subjects within twelve months.	12 months
Primary	Incidence of treatment procedure disruption	Proportion of test subjects terminating the treatment procedure after randomization by request due to unacceptable pain or discomfort during the procedure.	12 months
Secondary	Neuropathic Pain Symptoms Inventory (NPSI)	Numeric Rating Scale, range 0 (no pain) to 10 (worst pain imaginable) in whole numbers	Baseline, 1 and 3 moths after treatment
Secondary	Activities of daily life	Impact and intensity of pain categorically in 16 situations of daily life. Categorically reported as "Avoid", "Major restriction", "Some restriction", "Minor restriction", "No restriction" or "Do not perform"	Baseline, 1 and 3 months
Secondary	Patient's Global Impression of Change (PGIC)	Rating of global change perceived by the test subject from "More Worse" to "Much better" and a scale from 0 to 10.	1 and 3 months after treatment.
Secondary	Pain at rest, coughing and when active	Numeric Rating Scale, range 0 (no pain) to 10 (worst pain imaginable) in whole numbers	Weekly after treatment for three months
Secondary	General Health	Short form 36 Health Survey on physical, social and mental level of function on a score from 0 to 100.	Baseline, 1 and 3 months after treatment
Secondary	Pain at procedure	Evaluation of pain/discomfort at administration of BTX-A using subcutaneous injection in the skin of the chest wall. Numeric Rating Scale, range 0 (no pain) to 10 (worst pain imaginable) in whole numbers	Baseline