The Effect of Cooling Face Therapy on Recovery from Early Complications for Patients after Rhinoplasty

The Effect of Cooling Face Therapy on Recovery from Early Complications for Patients after Rhinoplasty: A Randomized Controlled Trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20230310057672N2

Enrollment

Registered

2024-03-23

Start date

2024-04-02

Completion date

Unknown

Last updated

2024-05-27

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

Conditions

Condition 1: Facial Pain (early postsurgical complication). Condition 2: Periorbital edema (early postsurgical complication). Condition 3: Facial ecchymosis. Atypical facial pain Edema of orbit Ecchymoses

Interventions

Intervention 1: Intervention group: After the patient has had a rhinoplasty and is in the surgical ward, waiting to removing from anesthesia, and showing signs of patient consciousness, the researche

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients who undergoing surgical rhinoplasty, agree to share in the study. who are 18-60 years old at the time of the data collection phase

Exclusion criteria

Exclusion criteria: Involvement with any other ongoing studies. Medically diagnosed with psycho-mental diseases. Patients with a previous surgical rhinoplasty procedure, patients with bleeding disorders as their condition interfere with the degree of intraoperative bleeding and affect the results as well as diabetic patients.

Design outcomes

Primary

Measure	Time frame
The primary outcome variable that may relieve or reduce the early complication (pain, edema and ecchymosis) after Rhinoplasty. Timepoint: The clinical intervention of the experiment is carried out 30 minutes after rhinoplasty for patients , the results of the intervention are shown to reduce the intensity of pain, edema and ecchymosis from the first day after surgery to the second day. The assesses the pain, edema and ecchymosis facial will occur after 4 hours and repeated in 24 hours for two groups. Method of measurement: Measurement method before and after clinical intervention using Numeric Pain Rating Scale (NPRS) to measure facial pain (Alghadir, A. H., Anwer, S., & Iqbal, Z. A. 2016). Modified Surgeon Periorbital Rating of Edema and Ecchymosis (SPREE) questionnaire to measure edema and ecchymosis (Kara, CO. and Gökalan, 1999).	—

Measure

Time frame

The primary outcome variable that may relieve or reduce the early complication (pain, edema and ecchymosis) after Rhinoplasty. Timepoint: The clinical intervention of the experiment is carried out 30 minutes after rhinoplasty for patients , the results of the intervention are shown to reduce the intensity of pain, edema and ecchymosis from the first day after surgery to the second day. The assesses the pain, edema and ecchymosis facial will occur after 4 hours and repeated in 24 hours for two groups. Method of measurement: Measurement method before and after clinical intervention using Numeric Pain Rating Scale (NPRS) to measure facial pain (Alghadir, A. H., Anwer, S., & Iqbal, Z. A. 2016). Modified Surgeon Periorbital Rating of Edema and Ecchymosis (SPREE) questionnaire to measure edema and ecchymosis (Kara, CO. and Gökalan, 1999).

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Countries

Iraq

Contacts

Public ContactAlaa Jawad Kadhim

University of Baghdad/College of Nursing

alaaj@conursing.uobaghdad.edu.iq+964 770 352 0314

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026