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Post-traumatic Facial EdemaNCT02977182

Lymphedema Treatment for Blunt Facial Trauma

A study testing Complete Decongestive Therapy (CDT) in people with Post-traumatic Facial Edema, run by Our Lady of the Lake Hospital at 1 site in United States.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Injuries to the face caused by traumatic events such as motor vehicle collisions, assault, and falls can result in facial trauma, which can result in swelling and disfiguration that impairs the important functions of the face, sometimes to a life threatening degree. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Post-traumatic Facial Edema
What is being tested?
Complete Decongestive Therapy (CDT)
Could I receive a placebo?
No, everyone receives an active treatment
How many people
50 participants
Where
1 siteUnited States
Study dates
Nov 2016to Nov 2018
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Adult trauma patients 18 years of age or older
  • Presence of facial trauma as determined by X-ray or computed tomography (CT)
  • Presence of face/neck lymphedema characterized as at least Stage 1 on the MD Anderson Cancer Center's Head and Neck Lymphedema (HNL) rating scale

Who cannot join

  • Less than 18 years of age
  • Presence of injury to the carotid artery or jugular veins
  • Presence of upper quadrant deep vein thrombosis
  • Presence of known infection
  • Unwilling or unable to consent (or unable to find an appropriate surrogate)
  • Pregnant
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  • Expected death within 24 hours of enrollment, or desire by patient of family to pursue palliative rather than aggressive, supportive care
  • Inability to speak English such that assessment of primary endpoints would not be feasible
  • Prisoners
  • Patients previously enrolled in another clinical trial

Trial locations and contacts

1 site in 1 country.

Danielle Tatum, PhD contact

2257656649

Danielle.Tatum@ololrmc.com

Jeffrey Gruner, MD, FACS contact

2257656893

Jeffrey.Gruner@ololrmc.com

United States1 site, 1 recruiting
  • Our Lady of the Lake Regional Medical Center

    Baton Rouge, Louisiana, 70808

    Danielle Tatum, Ph.D., 225-765-6649, Danielle.Tatum@ololrmc.com

    Hollis O'Neal, MD, MSc, 225-757-4070, honeal@lsuhsc.edu

    Recruiting

Other trials in United States

About this study

Official title: The Effect of Lymphedema Treatment for the Management of Blunt Facial Trauma

Injuries to the face caused by traumatic events such as motor vehicle collisions, assault, and falls can result in facial trauma, which can result in swelling and disfiguration that impairs the important functions of the face, sometimes to a life threatening degree. These injures and the resultant swelling can also precipitate psychological and social consequences.

Lymphedema is an abnormal amount of fluid that causes swelling, usually in the arms or legs. The most common presentation of lymphedema is in the upper extremities due to breast cancer treatment (Maclellean RA et al). As such, standards of care for management of lymphedema are primarily derived from the cancer research literature and involve the extremities (Moffatt CJ. 2003 QJM). The current gold standard treatment for patients with extremity lymphedema is complete decongestive therapy (CDT) (Zuther 2013). CDT is a multimodal therapy consisting of four components: manual lymph drainage, compression wrapping, exercise, and skin care (Zuther 2013).These same therapeutic techniques of CDT have been employed at Our Lady of the Lake Regional Medical Center (OLOLRMC) and adapted to treat patients with facial trauma with anecdotally good results primarily related to cosmesis. To the best of our knowledge, no clinical studies examining the effect of lymphedema treatment in the management of blunt facial trauma currently exist.. Beyond the consideration of cosmesis, we also seek to determine if this intervention improves clinical outcomes such as time to swallowing and reduced time utilizing mechanical ventilation. This study will prospectively evaluate the use of complete decongestive therapy to test the hypothesis that this intervention results in improved clinical outcomes in patients with blunt facial trauma.

Read the detailed description

Introduction The face is an anatomically complex structure, consisting of skin, muscles for both fine and gross motor functions, a complex bony structure, and vital sensory organs. These structures allow one to eat, breathe, see, hear, and speak. Injuries to the face caused by traumatic events such as motor vehicle collisions, assault, and falls can result in facial trauma, which can result in swelling and disfiguration that impairs the important functions of the face, sometimes to a life threatening degree. These injures and the resultant swelling can also precipitate psychological and social consequences.1-3 Lymphedema is an abnormal amount of fluid that causes swelling, usually in the arms or legs. Though lymphedema can occur as a result of trauma, it is most commonly associated with side effects of certain cancer-related treatments such as radiation therapy and lymph node removal. The most common presentation of lymphedema is in the upper extremities due to breast cancer treatment.4 As such, standards of care for management of lymphedema are primarily derived from the cancer research literature and involve the extremities.5 The current gold standard treatment for patients with extremity lymphedema is complete decongestive therapy (CDT).6 CDT is a multimodal therapy consisting of four components: manual lymph drainage, compression wrapping, exercise, and skin care.6 Manual lymph drainage (MLD) is a delicate form of massage designed to improve tissue and cellular health by facilitating fluid removal from edematous areas. Compression wrapping utilizes compression garments or short stretch compression bandages and is primarily used in the acute (or intensive) phase of CDT as a means to reinstate sufficient resistance to skin tissues whose elastic fibers are damaged by lymphedema. Exercise, especially when combined with compression, improves removal of fluid from the affected area. Finally, skin care treatments keep skin clean and moisturized to reduce infections that can occur with lymphedema.6 These same therapeutic techniques of CDT have been employed at Our Lady of the Lake Regional Medical Center (OLOLRMC) and adapted to treat facial edema in patients with facial trauma with anecdotally good results in terms of cosmesis. To the best of our knowledge, no clinical studies examining the effect of lymphedema treatment in the management of blunt facial trauma currently exist. Beyond the consideration of cosmesis, we also seek to determine if this intervention improves clinical outcomes such as time to swallowing and reduced time utilizing mechanical ventilation. This study will prospectively evaluate the use of complete decongestive therapy to test the hypothesis that this intervention results in improved clinical outcomes in patients with blunt facial trauma.

Specific Aims Specific Aim I: To determine whether complete decongestive therapy can significantly reduce facial lymphedema as measured by a previously established facial composite scoring protocol.

Specific Aim II: To determine whether complete decongestive therapy can improve clinical outcomes for patients with facial trauma Study Objective and Endpoints Study Objective The primary objective of this study is to determine the effect(s), if any, of complete decongestive therapy in the management of facial trauma.

Primary Endpoint The primary endpoint will be the composite facial score measured on the day of discharge from the Trauma Neuro Critical Care (TNCC) intensive care unit (ICU) at OLOLRMC. This measurement is based on the Head \& Neck Lymphedema (HNL) program at MD Anderson Cancer Center (MDACC) whose standard evaluation protocol includes specific point-to-point measurements of the face (Smith \& Lewin 2010; Smith and Lewin 2014). A series of key facial measurements are totaled to provide a "composite facial score". Based on the clinical experience at MDACC with more than 150 patients, their HNL program has developed criteria to define clinically detectable improvements in external HNL. Those criteria are a drop in lymphedema stage or a minimum threshold of 2% reduction in the composite measurement equating to at least a 2-cm change in absolute values (Smith \& Lewin 2014).

Secondary endpoints

Because the facial and neck composite scores only provide evaluation of the extent of edema, we also seek to assess patient outcomes with regards to the following:

  1. Stage of lymphedema as defined by the MDACC HNL edema rating scale
  2. Number of mechanical ventilation days
  3. Narcotic pain medicine utilization
  4. Steroid utilization
  5. Pain scale scores as determined by the Visual Analog Scale or the adult non-verbal pain score
  6. Time to swallowing
  7. ICU length of stay (ICULOS)
  8. Hospital length of stay (LOS)
Being tested
Complete Decongestive Therapy (CDT)

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Complete Decongestive Therapy (CDT)Other

    CDT is a multimodal therapy consisting of four components: manual lymph drainage, compression wrapping, exercise, and skin care

Study groups in NCT02977182
Study groupRoleWhat they receive
Control GroupNo interventionThe control group will receive standard speech therapy treatments but not lymphedema treatment and will serve as the baseline for comparison for assessment of the effects of CDT.
Active Treatment GroupExperimentalThe active treatment group will receive standard speech therapy treatments in addition to complete decongestive therapy from a certified Speech Language Pathologist (CCC-SLP) trained in CDT.
Receives: Other: Complete Decongestive Therapy (CDT)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Composite facial score

    This measurement is based on the Head \& Neck Lymphedema program at MD Anderson Cancer Center whose standard evaluation protocol includes specific point-to-point measurements of the face which are totaled to provide a composite facial score.

    Measured: Up to 2 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Nov 2016 (estimated)
  2. Study startNov 2016
  3. Primary completionNov 2018 (estimated)
  4. Study completionNov 2018 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
50 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02977182
Sponsor's protocol ID
9521
Status last verified
Nov 2016
First submitted
22 Nov 2016
Last updated
30 Nov 2016
Results posted
No
Data monitoring committee
No
Individual data sharing
No

Publications

  • Glynn SM, Asarnow JR, Asarnow R, Shetty V, Elliot-Brown K, Black E, Belin TR. The development of acute post-traumatic stress disorder after orofacial injury: a prospective study in a large urban hospital. J Oral Maxillofac Surg. 2003 Jul;61(7):785-92. doi: 10.1016/s0278-2391(03)00239-8.

    PubMed 12856251
  • Rankin M, Borah GL. Perceived functional impact of abnormal facial appearance. Plast Reconstr Surg. 2003 Jun;111(7):2140-6; discussion 2147-8. doi: 10.1097/01.PRS.0000060105.63335.0C.

    PubMed 12794453
  • Maclellan RA, Couto RA, Sullivan JE, Grant FD, Slavin SA, Greene AK. Management of Primary and Secondary Lymphedema: Analysis of 225 Referrals to a Center. Ann Plast Surg. 2015 Aug;75(2):197-200. doi: 10.1097/SAP.0000000000000022.

    PubMed 24691335
  • Glynn SM, Shetty V, Elliot-Brown K, Leathers R, Belin TR, Wang J. Chronic posttraumatic stress disorder after facial injury: a 1-year prospective cohort study. J Trauma. 2007 Feb;62(2):410-8; discussion 418. doi: 10.1097/01.ta.0000231556.05899.b0.

    PubMed 17297333
  • Moffatt CJ, Franks PJ, Doherty DC, Williams AF, Badger C, Jeffs E, Bosanquet N, Mortimer PS. Lymphoedema: an underestimated health problem. QJM. 2003 Oct;96(10):731-8. doi: 10.1093/qjmed/hcg126.

    PubMed 14500859
  • Cohen MD. Complete decongestive physical therapy in a patient with secondary lymphedema due to orthopedic trauma and surgery of the lower extremity. Phys Ther. 2011 Nov;91(11):1618-26. doi: 10.2522/ptj.20100101. Epub 2011 Aug 25.

    PubMed 21868611

Questions about this trial

What is this clinical trial studying?

A study testing Complete Decongestive Therapy (CDT) in people with Post-traumatic Facial Edema, run by Our Lady of the Lake Hospital at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 30 Nov 2016. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Danielle Tatum, PhD (2257656649, Danielle.Tatum@ololrmc.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Composite facial score (time frame: Up to 2 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02977182, which also lists 6 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Nov 2016.

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