Efficacy of low temperature tumescent solution in post operative outcome : A half-side comparison randomised controlled trial

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

TCTR

Registry ID

TCTR20180621001

Enrollment

Registered

2018-06-21

Start date

2018-06-25

Completion date

Unknown

Last updated

2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

patient who plan to do liposuction Tumescent &#44

Interventions

control > Room air temperature tumescent . ,Study cool : 4 degree celcius .

Experimental Procedure/Surgery,Experimental Procedure/Surgery

Room temp tumescent group,4 degree tumescent group

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patient who want to do liposuction ASA class 1 patient not on anti-coagulant

Exclusion criteria

Exclusion criteria: allergy to lidocaine on steriod

Design outcomes

Primary

Measure	Time frame
blood loss 1 month Degree of echymosis . Visual analog score	—

Secondary

Measure	Time frame
post operative pain 14 days Visual analog score	—

Countries

Thailand

Contacts

Public ContactChatchai Pruksapong

Phramongkutklao hospital

cpruksapong@hotmail.com0863178962

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026

Efficacy of low temperature tumescent solution in post operative outcome : A half&#45;side comparison randomised controlled trial