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RecruitingNCT07810179Updated Sep 9, 2026

Prospective Comparative Cohort Study of Premium Versus Economy Cabin Travel and Popliteal Vein Diameter After Long-Haul Flight After an Aesthetic Surgery

An observational study in Physiologic Venous Dilation and Air Travel, sponsored by Research Inc. Recruiting at 1 site in Colombia. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-09-09.

Sponsored by Research Inc · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
200
Ages
18 Years to 65 Years
Sex
All
01

Study summary

This prospective cohort study will compare popliteal vein diameter changes in international travelers who independently fly to Bogota in premium business/first class or economy class. Standardized bilateral ultrasound will be performed before flight, within 2 hours after arrival, and at 24 and 48 hours. The primary outcome is the adjusted between-group difference in change from preflight diameter to arrival. Travel behavior and venous-risk confounders will be measured prospectively.

Read the detailed description

Travelers with documented premium or economy itineraries will be enrolled before departure. Bilateral popliteal vein diameter and cross-sectional area will be measured using a standardized ultrasound protocol before flight and three times after arrival, all before surgery. Actual seat characteristics, flight duration, connections, ambulation, fluid intake, alcohol, sedatives, and compression stocking use will be recorded. Mixed-effects and propensity-weighted analyses will compare the magnitude and persistence of dilation between cabin groups while acknowledging that cabin class is not randomized.

02

Conditions studied

  • Physiologic Venous Dilation
  • Air Travel

Keywords

  • Cabin Class
  • Business Class
  • First Class
  • Economy Class
  • Popliteal Vein
  • Duplex Ultrasound
  • Medical Tourism
03

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adult international medical travelers with prebooked premium business/first-class or economy-class itineraries of at least 4 hours.

Inclusion criteria

  • Age 18 to 65 years.
  • Commercial flight to Bogota with at least 4 hours of total airborne time.
  • Prebooked premium business/first-class or economy-class seat documented before enrollment.
  • Standardized preflight ultrasound within 24 hours before departure.
  • Arrival, 24-hour, and 48-hour ultrasound completed before surgery.
  • Written informed consent.

Exclusion criteria

Exclusion Criteria:

  • Current or prior unprovoked deep venous thrombosis requiring therapeutic anticoagulation.
  • Therapeutic anticoagulation during the study window.
  • Current pregnancy.
  • Lower-extremity condition preventing standardized bilateral popliteal ultrasound.
  • Surgery, prolonged immobilization, or major intravenous fluid administration before completion of the 48-hour scan.
  • Use of cabin upgrade after baseline or inability to verify the actual cabin flown.
04

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
200 participants (estimated)
Target follow-up
1 Month
Patient registry
Yes

Groups and cohorts

  • Premium Cabin Travelers

    Participants who independently booked and completed the qualifying itinerary in business or first class.

    Other: Premium Cabin Air Travel Exposure · Diagnostic Test: Standardized Bilateral Popliteal Vein Ultrasound

  • Economy Cabin Travelers

    Participants who independently booked and completed the qualifying itinerary in economy or basic economy class.

    Other: Economy Cabin Air Travel Exposure · Diagnostic Test: Standardized Bilateral Popliteal Vein Ultrasound

Interventions

  • OtherPremium Cabin Air Travel Exposure

    Preexisting travel exposure defined by the cabin actually flown. Seat pitch, recline, lie-flat capability, aisle/window position, and ambulation opportunities will be recorded. Linked arm/group(s): Premium Cabin Travelers.

  • OtherEconomy Cabin Air Travel Exposure

    Preexisting economy-cabin exposure with documentation of seat characteristics, position, movement, hydration, and other travel behaviors. Linked arm/group(s): Economy Cabin Travelers.

  • Diagnostic testStandardized Bilateral Popliteal Vein Ultrasound

    Triplicate anteroposterior and transverse diameter and cross-sectional-area measurements in both legs after a standardized resting period, with compressibility and flow assessment. Linked arm/group(s): Premium Cabin Travelers, Economy Cabin Travelers.

05

What researchers measure

Primary outcomes

  1. Between-Cabin Difference in Change in Mean Bilateral Popliteal Vein Diameter

    Difference between premium and economy groups in the participant-level change from preflight baseline to arrival. Diameter will be the mean of triplicate anteroposterior measurements in both legs and will be reported in millimeters.

    Time frame: Within 24 hours before departure and within 2 hours after arrival at the study site. 3 days

Secondary outcomes

  1. Incidental Venous Thrombosis or Abnormal Compressibility

    Number and proportion with a new abnormality requiring immediate clinical assessment.

    Time frame: From preflight baseline through 48 hours after arrival. 3 days

06

Study locations

1 of 1 sites recruiting
07

References and documents

Publications

  • Ramirez B, Aguilar H, Stanford N, Paez Z, Menendez JP, Pachon J, Osorio E, Varela A. Aesthetic Surgical Tourism: Physiological Changes During Flight That May Affect Patient Safety and Outcomes. Plast Reconstr Surg Glob Open. 2026 May 8;14(5):e7568. doi: 10.1097/GOX.0000000000007568. eCollection 2026 May. PubMed 42110381 ↗
  • Hoyos AE, Ramirez B, Benavides J, Perez Pachon ME, Varela A. Aeromedical Considerations for Patient Safety in Aesthetic Medical Tourism. Aerosp Med Hum Perform. 2024 Oct;95(10):765-770. doi: 10.3357/AMHP.6432.2024. PubMed 39431700 ↗

Individual participant data

Plan to share: No — not contempled in the patient informed consent

08

Registry details

Key details

Study ID
NCT07810179
Lead sponsor
Research Inc
Responsible party
Sponsor
First posted
Sep 9, 2026
Start date
Jan 12, 2024
Primary completion
Sep 1, 2026
Completion
Dec 1, 2026 (estimated)
Last update
Sep 9, 2026

Study contacts

Hugo Aguilar, MD, Plastic surgeon
Contact
havplasticacademy@gmail.com
+57 301 6918526
Hugo Aguilar
principal investigator

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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