The Effect of Compression Stockings on Edema and Discomfort During Short Haul Flights

Sponsor
Herlev and Gentofte Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT03546725
Collaborator
(none)
34
1
2
3.5
9.7

Study Details

Study Description

Brief Summary

Compression stockings have beneficial effects on the development of venous thromboembolic complications and oedema during long- haul flights. A randomized controlled trial investigating the effect of compression stockings during short-haul flights with a duration less than fur ours is lacking. Deep vein thrombosis is very rare on flights shorter than four hours, but compression stocking could have beneficial effects on other outcomes. The aim of this study is to assess if compression stockings used during a 3-3.5-hour flight will decrease leg edema and discomfort.

Condition or Disease Intervention/Treatment Phase
  • Device: Compression stocking
N/A

Detailed Description

All participants will be adults who will undergo a 3-3.5 hours flight. Participants have received oral and written information about the trial. All compression stockings have a class two compression level (corresponding to 23-32 mmHg compression). Participants will be randomized to wear a compression stocking on one leg, while the other side acts as control. Within an hour preflight, the patient will measure ankle and calf circumference at marked circumferential areas on the leg and answer questionnaires regarding leg pain and subjective discomfort, whereafter the stocking will be put on, on the randomized side. Within one hour after the flight the stocking will be removed and patients will once again measure the ankle and calf circumference at the marked circumference and fill out the questionnaire.

Sample size: Mean difference in ankle circumference set to -0.19 cm. Standard deviation of the mean difference set to 0.3, 5% alfa and 80% power. Sample size with a paired design = at least 18 participants. However, for practical reasons we will include up to approximately 50 adults in the trial.

Withdrawal and dropout criteria: All participants can withdraw their consent at any point during the trial, without the need for explaining any reasons for withdrawal. Since compression stockings do not cause side effects, except for patients with severe arterial insufficiency in the legs, we do not expect the trial to be stopped due to complications. All withdrawals will be accounted for in the scientific publication.

Study Design

Study Type:
Interventional
Actual Enrollment :
34 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Participants will be randomised to wear a compression stocking on either the left or the right leg during a 3 - 3.5 hour flight. All participants will act as their own control, and as a result all data will be paired.Participants will be randomised to wear a compression stocking on either the left or the right leg during a 3 - 3.5 hour flight. All participants will act as their own control, and as a result all data will be paired.
Masking:
Single (Outcomes Assessor)
Masking Description:
Outcomes will be self-reported, and the author that assesses the outcomes and performs data analyses will be blinded.
Primary Purpose:
Prevention
Official Title:
The Effect of Compression Stockings on Edema and Discomfort During Short Haul Flights: A Randomized Controlled Trial
Actual Study Start Date :
Feb 8, 2018
Actual Primary Completion Date :
May 26, 2018
Actual Study Completion Date :
May 26, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Leg with compression stocking

Leg wearing compression stocking during the flight

Device: Compression stocking
Compression stocking with length below the knee and a class two compression level (corresponding to 23-32 mmHg compression).

No Intervention: Leg without compression stocking

Leg not wearing compression stocking during the flight

Outcome Measures

Primary Outcome Measures

  1. Ankle edema [Ankle circumference on the leg wearing a compression stocking and the leg not wearing compression stocking is measured up to one hour before, and one hour after flight.]

    Difference in ankle circumference pre- and post flight on the leg with and the leg without compression stocking.

Secondary Outcome Measures

  1. Calf edema [Calf circumference on the leg wearing a compression stocking and the leg not wearing compression stocking is measured up to one hour before, and one hour after flight.]

    Difference in calf circumference pre- and post flight on the leg with and the leg without compression stocking.

  2. Leg pain [Leg pain is reported up to one hour before, and one hour after flight.]

    Self-reported assessment of leg pain on a Visual Analogue Scale.

  3. Leg discomfort [Leg discomfort is reported up to one hour before, and one hour after flight.]

    Self-reported assessment of leg discomfort on a Visual Analogue Scale.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Adult participants ≥ 18 years of both sexes. Otherwise no restriction, since each participant acts as their own control.
Exclusion Criteria:
  • Any condition requiring compression stockings during short-haul flights. Severe arterial insufficiency in the lower extremities.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Center for Perioperative Optimisation, Department of Surgery, Herlev og Gentofte Hospital, University of Copenhagen Copenhagen Denmark 2730

Sponsors and Collaborators

  • Herlev and Gentofte Hospital

Investigators

  • Principal Investigator: Joachim HH Olsen, BScMed, Center for Perioperative Optimisation, Department of Surgery, Herlev og Gentofte Hospital, University of Copenhagen
  • Study Director: Stina Öberg, MD, Center for Perioperative Optimisation, Department of Surgery, Herlev og Gentofte Hospital, University of Copenhagen
  • Study Director: Jacob Rosenberg, MD, DMSc, Center for Perioperative Optimisation, Department of Surgery, Herlev og Gentofte Hospital, University of Copenhagen

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Joachim Hjalde Halmsted Olsen, Bachelor of Medical Science, Herlev and Gentofte Hospital
ClinicalTrials.gov Identifier:
NCT03546725
Other Study ID Numbers:
  • 8392100
First Posted:
Jun 6, 2018
Last Update Posted:
Jun 13, 2018
Last Verified:
Jun 1, 2018
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 13, 2018