Gingival InflammationPhase 4NCT07814898
Comparison Between the Effect of Triclosan Toothpaste and Chlorhexidine Mouthwash on Gingival Health in a Group of Fixed Orthodontic Patients: A Randomized Controlled Clinical Trial
A Phase 4 study testing Triclosan 0.3% toothpaste, sodium fluoride 0.24% toothpaste and Chlorhexidine 0.2% mouthwash in people with Gingival Inflammation, run by University of Science and Technology, Yemen at 1 site in Yemen.
Trial summary
Study Protocol Introduction Title of the research study Comparison Between the effect of Triclosan Toothpaste and chlorhexidine Mouthwash on Gingival Health in Fixed Orthodontic Patients :A randomization controlled clinical trial. Read more about this study
- Who is it for?
- Ages 18 to 35 yearsHealthy volunteers can take part
- Conditions the study is for
- Gingival Inflammation
- What is being tested?
- Triclosan 0.3% toothpaste, sodium fluoride 0.24% toothpaste and Chlorhexidine 0.2% mouthwash
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 60 participants
- Where
- 1 siteYemen
- Study dates
- 14 Feb 2026to 9 Aug 2026
- Phase
- Phase 4
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 35 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- Patient age 18-35 years old.
- Interested, cooperative fixed orthodontic patients who are aware of the importance of using toothpastes and mouthwash during orthodontic treatment.
- Patients who have good oral hygiene during orthodontic treatment.
- Medically fit patients who are not using any medical treatment that may affect periodontal health such as (antibiotic, phenytoin).
- Class I, II, III malocclusion with mild to moderate crowding.
Who cannot join
- - Patients with systemic disease affecting periodontal health such as (lichen planus, pemphigus)
- Smoker patients.
- Chewing qat patients.
Trial locations and contacts
1 site in 1 country.
About this study
Study Protocol Introduction Title of the research study Comparison Between the effect of Triclosan Toothpaste and chlorhexidine Mouthwash on Gingival Health in Fixed Orthodontic Patients :A randomization controlled clinical trial.
Background Orthodontic brackets and elastics might interfere with effective removal of dental plaque, thereby increasing the risk of gingivitis. The aim of this study to compare the effect of triclosan toothpaste and chlorhexidine mouthwash on gingival health in a group of fixed orthodontic patients.
Read more
Procedures Participant eligibility will be assessed based on a dental examination, medical history and inclusion and exclusion criteria.
Inclusion criteria:
- Patient age 18-35 years old.
- Orthodontic patient in leveling and alignment stage.
- Interested, cooperative fixed orthodontic patients who are aware of the importance of using toothpastes and mouthwash during orthodontic treatment.
- Patients who have good oral hygiene during orthodontic treatment.
- Medically fit patients who are not using any medical treatment that may affect periodontal health such as (antibiotic, phenytoin).
- Class I, II, III malocclusion with mild to moderate crowding.
Exclusion criteria:
- Patients with systemic disease affecting periodontal health such as (lichen planus, pemphigus)
- Smoker patients.
- Chewing qat patients. Eligible participants will be randomly assigned to one of three groups Group 1: will use Colgate Total® toothpaste containing sodium fluoride 0.24% and Triclosan 0.3% for one month twice a day.
Group 2: will use Maxfresh ® toothpaste containing sodium fluoride 0.24% in addition to Hexadyl® Chlorhexidine mouthwash for one month twice a day.
Group 3: will brush their teeth by Colgate Maxfresh ® toothpaste containing sodium fluoride 0.24% for 3 month twice a day.
The participant will be instructed to brush and rinse his or her teeth twice a day and they must follow orthodontic treatment instructions to maintain the braces.
The study will last for three month.
Read the detailed description
3.2 Study population The study population will include fixed orthodontic patients who visit the dental clinics in the College of Dentistry, University of Science and Technology, Sana'a University, and private dental clinics. 3.3 Sample size In this study, the sample size will be determined using a power calculation based on a previous study (Alavi et al. 2018). Their study found a significant difference in the dental plaque index between the Chlorhexidine and fluoride groups (0.003±0.06 vs.
0.249±0.21). To achieve a power of 80% and confidence interval of 95%, the study will need to include 7 participants in each group (https://www.openepi.com/SampleSize/SSPropor.htm).To increase the reliability of the study and to make comparisons with previous similar studies, a total of 10 participants will be included in each group. This will result in a total sample of 60 participants in the study.
Triclosan group (10 male, 10 female), CHX group (10 male, 10 female) and Controlled group (10 male, 10 female). 3.4 sample selection 3.4.1 Inclusion criteria:
- Patient age 18-35 years old.
- Interested, cooperative fixed orthodontic patients who are aware of the importance of using toothpastes and mouthwash during orthodontic treatment.
- Patients who have good oral hygiene during orthodontic treatment.
- Medically fit patients who are not using any medical treatment that may affect periodontal health such as (antibiotic, phenytoin).
- Class I, II, III malocclusion with mild to moderate crowding. 3.4.2 Exclusion criteria:
- Patients with systemic disease affecting periodontal health such as (lichen planus, pemphigus)
- Smoker patients.
- Chewing qat patients. 3.5 study groups: The participants will be selected according to inclusion \&exclusion criteria and they will be divided in to three groups and will be given instructions as follows:
- Group I (Triclosan group): will brush their teeth by Colgate Total® toothpaste containing sodium fluoride 0.24% and Triclosan 0.3% for 3 month twice a day.
- Group II (CHX group): will brush their teeth by Colgate maxfresh ® toothpaste containing sodium fluoride 0.24% in addition to Hexadyl® Chlorhexidine mouthwash for 3 month twice a day.
- Group III (Controlled group): will brush their teeth by Colgate maxfresh ® toothpaste containing sodium fluoride 0.24% for 3 month twice a day. The selected toothpaste and mouthwash will be provided for all participants free of charge.
3.6 Clinical examination, Measurement, procedure: Clinical examination will be performed for Triclosan group and CHX group participants in dental unit. Teeth and gingiva will be dried and examined under adequate light, using a mouth mirror and periodontal probe. Before the beginning of examination, all of the selected participants will be instructed on tooth brushing technique (bass technique) and flossing. Scaling and polishing will be performed 2 weeks prior to the beginning of the study. Patients who will fail to maintain good oral hygiene will be excluded from the study.
The measurement will be done on teeth selected according to the proposal method for plaque index, gingival index. Patients should brush and rinse their teeth twice a day and they must follow orthodontic treatment instructions to maintain their fixed orthodontic appliance. Each patient will be informed to brush twice daily with the assigned toothpaste and will be provided with a follow up chart each visit where the dentist will assess the compliance of the patients. The patients will mark in the follow up chart each time they brush their teeth. 3.6.1 follow up time: To detect a clinically meaningful reduction in plaque index from baseline to 3 months among the study groups (Boneta A, Aguilar M, Romeu F, Stewart B, DeVizio W,
Proskin H.) clinical examination will be in three period of time: Initial examination (T0):
will be performed at the beginning of the study, before orthodontic treatment and after scaling and polishing and oral hygiene instruction. First examination (T1): will be performed 1 month after fixed orthodontic appliance is inserted. Secondary examination (T2): will be performed 2 months after fixed orthodontic appliance is inserted. Final examination(T3): will be performed 3 months after fixed orthodontic appliance is inserted.
3.6 Randomization This study will be a randomized controlled clinical trial design to compare between Triclosan toothpaste and Chlorhexidine mouthwash on gingival health. The sample will be randomly divided into three groups by using the sealed envelope technique to achieve random allocation to the study groups. Each envelope will be numberd from 1 to 60 and papers will be written to be inserted inside the envelope with the name of each group (Triclosan group, CHX group or controlled group) according to the number of samples for each group (20 paper for Triclosan group ,20 paper for CHX group 20 paper for controlled group). Each participant will choose an envelope and the assistant will record each participant's result and keep it in list to know the participants of each group and give each participant the necessary instructions for his/her group. 3.7 Blinding This study will be double-blind study the researcher and statistician will not be able to know who the participants are in each group. There will be a supervisor to help in divide the groups, give instruction, and record the results. participants will be aware of the product being used because it is difficult to hide the toothpaste and mouthwash containers.
This rigorous approach reduces potential biases and enhances the scientific validity of the study.
- Conditions
- Gingival Inflammation
- Being tested
- Triclosan 0.3% toothpaste, sodium fluoride 0.24% toothpaste, Chlorhexidine 0.2% mouthwash
- Medical subject headings
- Gingivitis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Triclosan 0.3% toothpasteDrug
participant will brush their teeth with triclosan and sodium fluoride toothpaste twice daily
sodium fluoride 0.24% toothpasteDrug
participant will brush their teeth twice daily
Chlorhexidine 0.2% mouthwashDrug
participant will brush and rinse their teeth with CHX mouthwash and sodium fluoride toothpaste
| Study group | Role | What they receive |
|---|---|---|
| Triclosan toothpaste with sodium fluoride | Experimental | participants will brush their teeth twice daily Receives: Drug: Triclosan 0.3% toothpaste |
| CHX Mouthwash Group with sodium fluoride toothpaste | Experimental | participants will brush and rinsing their teeth twice daily Receives: Drug: Chlorhexidine 0.2% mouthwash |
| control Group sodium fluoride toothpaste | Active comparator | participants will brush their teeth twice daily Receives: Drug: sodium fluoride 0.24% toothpaste |
What is being measured
The primary outcome is the main question the study is designed to answer.
gingival index
evaluation of gingival index using the Loe and Sinless gingival index
Measured: at baseline, one month, two months, three months.
Secondary outcomes (1)
plaque index
evaluation of dental plaque accumulation using Loe and Sinless plaque index
Measured: at baseline, one month, two months, three months.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Sep 2026
- Study start14 Feb 2026
- Primary completion9 May 2026
- Study completion9 Aug 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Gingival InflammationStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 4
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Sequential
- Model description
- The participants will be selected according to inclusion \&exclusion criteria and they will be divided in to three groups and will be given instructions as follows: * Group I (Triclosan group): will brush their teeth by Colgate Total® toothpaste containing sodium fluoride 0.24% and Triclosan 0.3% for 3 month twice a day. * Group II (CHX group): will brush their teeth by Colgate maxfresh ® toothpaste containing sodium fluoride 0.24% in addition to Hexadyl® Chlorhexidine mouthwash for 3 month twice a day. * Group III (Controlled group): will brush their teeth by Colgate maxfresh ® toothpaste containing sodium fluoride 0.24% for 3 month twice a day. The selected toothpaste and mouthwash will be provided for all participants free of charge. Figure (
- Masking
- Double blind
- Who is masked
- Investigator, Outcomes assessor
- Enrolment
- 60 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Science and Technology, Yemen
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Fatimah Alzahra Alwane, University of Science and Technology, Yemen
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07814898
- Sponsor's protocol ID
- 1447/0090/UREC/UST
- Status last verified
- Sep 2026
- First submitted
- 5 Sep 2026
- Last updated
- 11 Sep 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: individual participant data will not be shared to protect patient privacy and confidentiality
Study at a glance
From the registry record, last updated by the sponsor on 11 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparison Between the Effect of Triclosan Toothpaste and Chlorhexidine Mouthwash on Gingival Health in a Group of Fixed Orthodontic Patients: A Randomized Controlled Clinical Trial
- ClinicalTrials.gov ID
- NCT07814898
- Acronym / sponsor ID
- 1447/0090/UREC/UST
- Conditions
- Gingival Inflammation
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 60 participants (actual)
- Lead sponsor
- University of Science and Technology, YemenUniversity, hospital or other
- Study start
- 14 Feb 2026 (actual)
- Primary completion
- 9 May 2026 (actual)
- Study completion
- 9 Aug 2026 (actual)
- First posted
- 11 Sep 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Study Protocol Introduction Title of the research study Comparison Between the effect of Triclosan Toothpaste and chlorhexidine Mouthwash on Gingival Health in Fixed Orthodontic Patients :A randomization controlled clinical trial.
Background Orthodontic brackets and elastics might interfere with effective removal of dental plaque, thereby increasing the risk of gingivitis. The aim of this study to compare the effect of triclosan toothpaste and chlorhexidine mouthwash on gingival health in a group of fixed orthodontic patients.
Procedures Participant eligibility will be assessed based on a dental examination, medical history and inclusion and exclusion criteria.
Inclusion criteria:
- Patient age 18-35 years old.
- Orthodontic patient in leveling and alignment stage.
- Interested, cooperative fixed orthodontic patients who are aware of the importance of using toothpastes and mouthwash during orthodontic treatment.
- Patients who have good oral hygiene during orthodontic treatment.
- Medically fit patients who are not using any medical treatment that may affect periodontal health such as (antibiotic, phenytoin).
- Class I, II, III malocclusion with mild to moderate crowding.
Exclusion criteria:
- Patients with systemic disease affecting periodontal health such as (lichen planus, pemphigus)
- Smoker patients.
- Chewing qat patients. Eligible participants will be randomly assigned to one of three groups Group 1: will use Colgate Total® toothpaste containing sodium fluoride 0.24% and Triclosan 0.3% for one month twice a day.
Group 2: will use Maxfresh ® toothpaste containing sodium fluoride 0.24% in addition to Hexadyl® Chlorhexidine mouthwash for one month twice a day.
Group 3: will brush their teeth by Colgate Maxfresh ® toothpaste containing sodium fluoride 0.24% for 3 month twice a day.
The participant will be instructed to brush and rinse his or her teeth twice a day and they must follow orthodontic treatment instructions to maintain the braces.
The study will last for three month.
Detailed description
3.2 Study population The study population will include fixed orthodontic patients who visit the dental clinics in the College of Dentistry, University of Science and Technology, Sana'a University, and private dental clinics. 3.3 Sample size In this study, the sample size will be determined using a power calculation based on a previous study (Alavi et al. 2018). Their study found a significant difference in the dental plaque index between the Chlorhexidine and fluoride groups (0.003±0.06 vs.
0.249±0.21). To achieve a power of 80% and confidence interval of 95%, the study will need to include 7 participants in each group (https://www.openepi.com/SampleSize/SSPropor.htm).To increase the reliability of the study and to make comparisons with previous similar studies, a total of 10 participants will be included in each group. This will result in a total sample of 60 participants in the study.
Triclosan group (10 male, 10 female), CHX group (10 male, 10 female) and Controlled group (10 male, 10 female). 3.4 sample selection 3.4.1 Inclusion criteria:
- Patient age 18-35 years old.
- Interested, cooperative fixed orthodontic patients who are aware of the importance of using toothpastes and mouthwash during orthodontic treatment.
- Patients who have good oral hygiene during orthodontic treatment.
- Medically fit patients who are not using any medical treatment that may affect periodontal health such as (antibiotic, phenytoin).
- Class I, II, III malocclusion with mild to moderate crowding. 3.4.2 Exclusion criteria:
- Patients with systemic disease affecting periodontal health such as (lichen planus, pemphigus)
- Smoker patients.
- Chewing qat patients. 3.5 study groups: The participants will be selected according to inclusion \&exclusion criteria and they will be divided in to three groups and will be given instructions as follows:
- Group I (Triclosan group): will brush their teeth by Colgate Total® toothpaste containing sodium fluoride 0.24% and Triclosan 0.3% for 3 month twice a day.
- Group II (CHX group): will brush their teeth by Colgate maxfresh ® toothpaste containing sodium fluoride 0.24% in addition to Hexadyl® Chlorhexidine mouthwash for 3 month twice a day.
- Group III (Controlled group): will brush their teeth by Colgate maxfresh ® toothpaste containing sodium fluoride 0.24% for 3 month twice a day. The selected toothpaste and mouthwash will be provided for all participants free of charge.
3.6 Clinical examination, Measurement, procedure: Clinical examination will be performed for Triclosan group and CHX group participants in dental unit. Teeth and gingiva will be dried and examined under adequate light, using a mouth mirror and periodontal probe. Before the beginning of examination, all of the selected participants will be instructed on tooth brushing technique (bass technique) and flossing. Scaling and polishing will be performed 2 weeks prior to the beginning of the study. Patients who will fail to maintain good oral hygiene will be excluded from the study.
The measurement will be done on teeth selected according to the proposal method for plaque index, gingival index. Patients should brush and rinse their teeth twice a day and they must follow orthodontic treatment instructions to maintain their fixed orthodontic appliance. Each patient will be informed to brush twice daily with the assigned toothpaste and will be provided with a follow up chart each visit where the dentist will assess the compliance of the patients. The patients will mark in the follow up chart each time they brush their teeth. 3.6.1 follow up time: To detect a clinically meaningful reduction in plaque index from baseline to 3 months among the study groups (Boneta A, Aguilar M, Romeu F, Stewart B, DeVizio W,
Proskin H.) clinical examination will be in three period of time: Initial examination (T0):
will be performed at the beginning of the study, before orthodontic treatment and after scaling and polishing and oral hygiene instruction. First examination (T1): will be performed 1 month after fixed orthodontic appliance is inserted. Secondary examination (T2): will be performed 2 months after fixed orthodontic appliance is inserted. Final examination(T3): will be performed 3 months after fixed orthodontic appliance is inserted.
3.6 Randomization This study will be a randomized controlled clinical trial design to compare between Triclosan toothpaste and Chlorhexidine mouthwash on gingival health. The sample will be randomly divided into three groups by using the sealed envelope technique to achieve random allocation to the study groups. Each envelope will be numberd from 1 to 60 and papers will be written to be inserted inside the envelope with the name of each group (Triclosan group, CHX group or controlled group) according to the number of samples for each group (20 paper for Triclosan group ,20 paper for CHX group 20 paper for controlled group). Each participant will choose an envelope and the assistant will record each participant's result and keep it in list to know the participants of each group and give each participant the necessary instructions for his/her group. 3.7 Blinding This study will be double-blind study the researcher and statistician will not be able to know who the participants are in each group. There will be a supervisor to help in divide the groups, give instruction, and record the results. participants will be aware of the product being used because it is difficult to hide the toothpaste and mouthwash containers.
This rigorous approach reduces potential biases and enhances the scientific validity of the study.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Sequential
- Masking
- Double blind (investigator, outcomes assessor)
- Number of arms
- 3
- Model description
- The participants will be selected according to inclusion \&exclusion criteria and they will be divided in to three groups and will be given instructions as follows: * Group I (Triclosan group): will brush their teeth by Colgate Total® toothpaste containing sodium fluoride 0.24% and Triclosan 0.3% for 3 month twice a day. * Group II (CHX group): will brush their teeth by Colgate maxfresh ® toothpaste containing sodium fluoride 0.24% in addition to Hexadyl® Chlorhexidine mouthwash for 3 month twice a day. * Group III (Controlled group): will brush their teeth by Colgate maxfresh ® toothpaste containing sodium fluoride 0.24% for 3 month twice a day. The selected toothpaste and mouthwash will be provided for all participants free of charge. Figure (
| Arm | Type | Receives |
|---|---|---|
| Triclosan toothpaste with sodium fluoride | Experimental | Drug: Triclosan 0.3% toothpasteparticipants will brush their teeth twice daily |
| CHX Mouthwash Group with sodium fluoride toothpaste | Experimental | Drug: Chlorhexidine 0.2% mouthwashparticipants will brush and rinsing their teeth twice daily |
| control Group sodium fluoride toothpaste | Active comparator | Drug: sodium fluoride 0.24% toothpasteparticipants will brush their teeth twice daily |
Who may qualify
- Ages
- 18 to 35 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (5 listed)
- Patient age 18-35 years old.
- Interested, cooperative fixed orthodontic patients who are aware of the importance of using toothpastes and mouthwash during orthodontic treatment.
- Patients who have good oral hygiene during orthodontic treatment.
- Medically fit patients who are not using any medical treatment that may affect periodontal health such as (antibiotic, phenytoin).
- Class I, II, III malocclusion with mild to moderate crowding.
Key exclusion criteria (3 listed)
- - Patients with systemic disease affecting periodontal health such as (lichen planus, pemphigus)
- Smoker patients.
- Chewing qat patients.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Triclosan 0.3% toothpasteparticipant will brush their teeth with triclosan and sodium fluoride toothpaste twice daily | Drug | Triclosan toothpaste with sodium fluoride |
| sodium fluoride 0.24% toothpasteparticipant will brush their teeth twice daily | Drug | control Group sodium fluoride toothpaste |
| Chlorhexidine 0.2% mouthwashparticipant will brush and rinse their teeth with CHX mouthwash and sodium fluoride toothpaste | Drug | CHX Mouthwash Group with sodium fluoride toothpaste |
Primary outcome
gingival index
Time frame: at baseline, one month, two months, three months.
evaluation of gingival index using the Loe and Sinless gingival index
1 secondary outcome
plaque index
Time frame: at baseline, one month, two months, three months.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 Sep 2026.
- Individual participant dataSharing planned: No. individual participant data will not be shared to protect patient privacy and confidentiality
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing Triclosan 0.3% toothpaste, sodium fluoride 0.24% toothpaste and Chlorhexidine 0.2% mouthwash in people with Gingival Inflammation, run by University of Science and Technology, Yemen at 1 site in Yemen.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 11 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Yemen. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
gingival index (time frame: at baseline, one month, two months, three months.). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Sep 2026.