ClinicalTrials.Veeva

Menu

Bromelain for Post-surgery Facial Swelling

M

Mohamed Bazina

Status

Enrolling

Conditions

Malocclusion

Treatments

Dietary Supplement: Bromelain

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The goal of this clinical trial is to learn if Bromelain Supplement works to decrease the amount of swelling or the amount of time swelling is present following jaw surgery. It will also learn about the safety of Bromelain supplement. The main questions it aims to answer are:

Does Bromelain decrease facial swelling following orthognathic, or jaw, surgery? Does Bromelain supplement decrease the amount of time that patients are swollen following orthognathic, or jaw, surgery?

Participants will:

Take Bromelain supplement once daily for 9 days total. Take 2 days before surgery and 7 days following surgery.

Keep a log of when the bromelain supplement is taken as well as another other medications.

Visit the clinic with pre and post surgical protocol

Enrollment

200 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • undergoing orthognathic surgery

Exclusion criteria

  • craniofacial anomalies
  • incomplete patient data
  • systemic disease that could affect healing
  • allergy to latex or pineapple
  • under 18 years of age
  • non english speaking

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

200 participants in 2 patient groups

Bromelain Supplement
Experimental group
Description:
1000mg bromelain supplement once a day, 2 days prior to and 7 days following surgery
Treatment:
Dietary Supplement: Bromelain
Control
No Intervention group
Description:
Standard of care

Trial contacts and locations

1

Loading...

Central trial contact

Emma E Palmer, DMD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems