Botox in the Healing of Surgical Wounds of the Neck

The recruitment status of this study is unknown because the information has not been verified recently.
Verified August 2010 by Capital District Health Authority, Canada.
Recruitment status was  Not yet recruiting
Sponsor:
Collaborator:
Allergan
Information provided by:
Capital District Health Authority, Canada
ClinicalTrials.gov Identifier:
NCT01177358
First received: July 8, 2010
Last updated: August 6, 2010
Last verified: August 2010

July 8, 2010
August 6, 2010
August 2010
August 2011   (final data collection date for primary outcome measure)
Vancouver Scar Scale [ Time Frame: 6 months ] [ Designated as safety issue: No ]
The surgeon will assess the healing of the surgical incision at 6 months and fill out the Vancouver Scar Scale following the operation.
Same as current
Complete list of historical versions of study NCT01177358 on ClinicalTrials.gov Archive Site
  • Patient and Observer Scar Assessment Scale [ Time Frame: 4 weeks ] [ Designated as safety issue: No ]
    The surgeon and the patient will be asked to fill out the survey at 4 weeks following the operation.
  • Patient and Observer Scar Assessment Scale [ Time Frame: 6 months ] [ Designated as safety issue: No ]
    The surgeon and the patient will be asked to fill out the survey at 6 months following the operation.
  • Vancouver Scar Scale [ Time Frame: 4 weeks ] [ Designated as safety issue: No ]
    The surgeon will assess the healing of the surgical incision and fill out the Vancouver Scar Scale at 4 weeks following the operation.
Same as current
Not Provided
Not Provided
 
Botox in the Healing of Surgical Wounds of the Neck
Botulinum Toxin A in the Healing of Surgical Wounds of the Neck: a Randomized, Prospective, Placebo-controlled Trial

The investigators hypothesize that Botox A will reduce scarring and improve healing of surgical neck wounds.

Botulinum Toxin A is a toxin produced by the anaerobic bacterial species Clostridium botulinum. The toxin specifically inhibits release of the neurotransmitter Acetylcholine at synaptic junctions, thus preventing neuromuscular transmission, and inducing paralysis of the muscle.

Previous studies have indicated that tensile forces on the skin may affect the healing of a wound. These forces act against the immature collagen laid down during wound healing and may stimulate overgrowth, thereby contributing to the formation of hypertrophic scars or keloids.

Using botox to paralyse the underlying muscles may reduce the tensile force on the overlying skin, and thus reduce scar formation and promote healing. Botox has also been shown to affect the cell cycle distribution of fibroblasts derived from hypertrophic scars.

The objective of this study is to determine the effects of BTX-A in wound healing and the reduction of scar formation.

Patients undergoing a thyroidectomy or parathyroidectomy will be randomized to receive either BTX-A injections along the surgical site or placebo immediately following closure. All incisions will be sutured in a similar fashion. BTX-A or normal saline will then be injected along the platysma muscle. The patient and the surgeon will be blinded to the treatment arm. Photographs will be taken of the surgical site at 4 weeks and 6 months. The patient and two otolaryngologists will independently score the healing of the wound using a standardized scoring method. The scores be compared between the two surgeons to determine correspondence and interobserver reliability.

The scores of the two treatment arms will be compared to reveal the effect of BTX-A on wound healing.

Interventional
Phase 2
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Prevention
Scar
  • Drug: Botulinum Toxin Type A

    A vial of Botulinum Toxin A containing 100U of Botox will be reconstituted with 2mL of normal saline for a concentration of 50U/mL.

    5 units (0.1mL) of Botulinum Toxin a will be injected at midline and 1.5cm lateral to midline, bidirectionally, following a thyroidectomy or parathyroidectomy.

    Other Names:
    • Allergan Botox
    • Drug Identification Number 01981501
  • Drug: Normal Saline
    0.1mL of normal saline in a placebo vial containing 2mL of normal saline will be injected along three sites (midline and 1.5cm lateral from midline) following a thyroidectomy or parathyroidectomy.
  • Experimental: Botulinum Toxin A injection

    A vial of Botulinum Toxin A containing 100U of Botox will be reconstituted with 2mL of normal saline for a concentration of 50U/mL.

    5 Units (0.1 mL) of Botulinum Toxin A will be injected at three sites along the incision (midline and 1.5 cm lateral to midline) following a thyroidectomy or parathyroidectomy.

    Intervention: Drug: Botulinum Toxin Type A
  • Placebo Comparator: Saline
    0.1 mL of normal saline in a placebo vial containing 2 mL of normal saline will be injected along the incision (midline and 1.5 cm lateral to midline) following a thyroidectomy or parathyroidectomy.
    Intervention: Drug: Normal Saline

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Not yet recruiting
100
February 2012
August 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • all patients referred to the ENT clinic for a thyroidectomy or parathyroidectomy

Exclusion Criteria:

  • patients with missing information, including demographic information
  • patients lost to follow up or have been followed for less than 6 months
  • patients with known allergy to lidocaine
  • patients in whom botox would be contraindicated in:
  • known history of neuromuscular disorders (myasthenia gravis, amyotrophic lateral sclerosis, Eaton-Lambert syndrome)
  • pregnant women
  • known allergy to botox, albumin
Both
18 Years and older
Yes
Contact: Elaine W Fung, BSc, MD 1-902-412-1240 elaine.fung@dal.ca
Canada
 
NCT01177358
BTX-001
No
Dr. Mark Taylor, CDHA, Department of Surgery, Division of Otolaryngology-Head and Neck Surgery
Capital District Health Authority, Canada
Allergan
Principal Investigator: Mark Taylor, FRCS Capital District Health Authority Nova Scotia
Capital District Health Authority, Canada
August 2010

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP