Accuracy of Stackable GuideNCT05617443
DLP Versus SLM Stackable Surgical Guide
A study testing stackable guide in people with Accuracy of Stackable Guide, run by Suez Canal University at 1 site in Egypt.
Trial summary
Purpose; The purpose of this research is to make a comparative estimation for the positional accuracy of dental implants inserted by selective laser melting and digital light processed computerized stackable surgical guides for patients with maxillary terminal dentitions. Read more about this study
- Who is it for?
- Ages 45 to 75 years
- Conditions the study is for
- Accuracy of Stackable Guide
- What is being tested?
- stackable guide
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 4 participants
- Where
- 1 siteEgypt
- Study dates
- 5 Oct 2022to 10 Jan 2023
- Phase
- Interventional
- 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 45 to 75 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- well healthy patients
- patients with maxillary terminal dentition
Who cannot join
- Patients with, systemic disease that might complicate post-operative healing or contribute to bone resorption
- patients with parafunctional habits, poor oral hygiene, limited mouth opening, severe alveolar bone deficiencies,
- patients with uncontrolled diabetes, current irradiation to the head or neck, psychological disorders, or alcohol, tobacco, or drug abuse
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Comparative Assessment For The Positional Accuracy Of Dental Implants Inserted By Computerized Stackable Surgical Guides Made From Selective Laser Melting And Digital Light Processing Technologies
Purpose; The purpose of this research is to make a comparative estimation for the positional accuracy of dental implants inserted by selective laser melting and digital light processed computerized stackable surgical guides for patients with maxillary terminal dentitions.
Materials and methods; Twenty-four dental implants will be installed in partially edentulous patients who will be applied for treatment of tooth loss and required fixed prosthodontic rehabilitation. Virtually designed prosthetically driven fixation base with its stackable surgical osteotomy guide will be used for bone reduction after tooth extraction and osteotomy preparation respectively. The inserted implants will be divided equally into two groups according to stackable surgical osteotomy guide to either selective laser melting (SLM) CO-Cr metal or digital light processing (DLP) surgical-guides. The final actual implant position will be compared to the preoperative planned position and the deviations will be calculated for coronal deviation, apical deviation in mm, and two angular deviation measurements in degrees.
Read the detailed description
Preoperative evaluation:
intra-oral and extra-oral examination and medical history for each patient will be recorded to assure that the patient will be eligible for the research.
Written informed consent will be assigned by the patients who will be included in the study.
Preoperative records Polyvinyl siloxane (PVS) impressions for both arches will be made. Also, an interocclusal record will be recorded.
The poured upper and lower cast will be mounted on the articulator and will be scanned using a tabletop scanner (DOF swing, DOF, Korea). the scanned file will be saved in stl format Clinical digital photographs for digital smile design will be used to generate a smile design driven by an individual's face and smile display. As such, it is critical to have at least two portraits representing the lips at rest and another one for a broad smile For each patient, a preoperative cone beam computed tomography (CBCT) scan with the two jaws separated via cotton rolls to separate the volume of interest using a CBCT machine (Scanora 3Dx, Soredex- Finland ) will be taken and saved as Digital Imaging and Communication in Medicine (DICOM) files. The saved STL files will be imported into computer-aided design (CAD) software ( Implastation, prodigident, USA) and superimpose these files to the DICOM files and the JPEG photo files.
Implant and prosthesis planning Virtual tooth setup of the desired prosthetic outcome can be designed to achieve true, restoratively driven implant placement when applied to 3-D surface DICOM data. Performing this virtual wax-up will be done by selecting and importing maxillary teeth from the software library, followed by adjustment of each tooth shape and position according to the patient's occlusion, gender, and smile. The final plan often requires bone reduction to facilitate implant placement and the necessary restorative space for the prosthesis.
A 3-dimensional implant planning using a Software Planning program (Implastation, ProDigident, USA), allows the clinicians to evaluate the osseous tissues concerning the ideal prosthetic position of the virtual waxed-up maxillary teeth. From this information, the sizes and implant receptor sites will be digitally evaluated in all of the necessary views, including cross-sectional, coronal, sagittal, and axial sections followed by virtual placement of the implants.
The stackable guide that will be planned to transfer the virtual plan to the operating field intraorally and consists of 3 components:
- carrier guide: it takes its support from the remaining dentition and has a foundation base attached to it by locks. its function is to transfer the foundation base to its accurate place in the patient mouth.
- foundation base: fixed to bone along the whole surgery time by fixation pins and has locks to be attached with subsequent osteotomy guides.
- osteotomy guide: contains the hole through which the implant drilling will be guided.
The outline of the surgical guide will be determined. and then the thickness and path of insertion. the amount of bone to be reduced will be determined .. a tooth-supported carrier (pin guide) will be designed, it takes its support from the remaining dentition. height of the foundation guide and locations of widely separated 4 anchor pins will be planned so that anchor pins help in achieving the highest degree of surgical accuracy, and then a tooth-supported carrier (pin guide) will be designed, it takes its support from the remaining dentition and accurately replicates the position of the anchor pins for subsequent guides, hence ensuring an accurate replication of the guide position.
With this protocol, teeth removal and bone reduction will be done virtually to provide the available restorative space (from the crest of the bone to the proposed incisal edge position and posterior occlusal plane).
Sleeveless osteotomy guide holes and offset will be designed corresponding to the guided drill kit that will be used(OGS guided kit, oxy implant, Italy) Finally, all guides will be exported as standard triangle language (STL) files and sent to additively manufactured machines.
Grouping:
The inserted implants will be divided equally into two groups according to the stackable surgical osteotomy guide fabrication/printing technique:
First group; in which implants will be placed using selective laser melting (SLM) CO-Cr metal surgical-guides Second group; in which implants will be placed using digital light processing (DLP) resin surgical-guides
Surgical stents fabrication:
For Digital light processing (DLP): DLP printers have a digital projector screen used to flash a single image of each layer on the entire platform at once using curable photopolymer resin. A vat of liquid photopolymer will be exposed to UV light from a digital projector under safelight conditions. The printer (Photon, Anycubic, China) builds the stent one layer at a time by tracing a laser beam on the surface of a vat of printable Resin liquid (SG resin, pro shape, turkey). The process will be repeated, forming another layer on top of the previous layer. This process continues layer by layer until the stent is completed. Printing will be started with a build angle of 45 and the printing thickness on the z-axis was set at 100 microns. After printing, the supports will be removed and the printed stents will be cleaned in an ultrasonic bath with ethyl alcohol for 2 minutes to remove excess resin. Stents will be post-polymerized for 30 minutes using an ultraviolet polymerization unit (bre. Lux power Unit 2, Bredent, Germany).
Regarding Selective Laser Melting (SLM); the STL file will be segmented into cross-sectional layer representations and then exported to a metal laser melting machine (vm120, Vulcan tech, Germany). To fabricate the prototype, this automated printing machine received numerical inputs of the surgical stent design. Sintering of the powder alloy (Starbond easy Pulver 30, Scheftner dental, Germany) to the predesigned guide via high-energy laser beams that traced across a powder bed of densely compacted powdered material, resulting in local melting and fusing of the particles. According to the 3D data fed into the machine, metallic powders will melt together, in a layer-by-layer strategy, creating three-dimensional objects.
Laser spot diameter of 0.08-0.1 mm, sintering speed of 1100-1200 mm/s, a layer thickness of 0.02 mm, and printing angle of 45 degrees, will be considered the parameters of the laser melting machine that will be used for the SLM stent fabrication. SLM stents will be extracted from the base plate and homogenization treatment will be performed at 1150ᵒ C for 30 minutes.
Surgical phase All surgeries will be performed by the same operator under complete aseptic conditions. The patients will be locally anesthetized.
Utilizing the existing dentition to position carrier resin guide to which everything else will be related. Verification of the carrier guide of the pin guide over the teeth will be done.
After verification, the carrier will be securely locked to the foundation metal printed guide and delivered over the teeth. This method allows for the metal foundation guide to be correctly positioned. Four anchor pins will be utilized to stabilize the metal foundation guide (divided equally into anterior and posterior regions bilaterally). An anchoring twist drill will be used with copious irrigation for the preparation of the fixation screw pathway. After that, four anchoring screws will be driven in the anterior and posterior areas After the FG will be secured to the bone, the pin guide will be removed, leaving the maxillary teeth available for extraction. The teeth will be all carefully removed, leaving the remaining alveolus exposed. The outer aspect of the metal FG will be used to determine the amount of bone reduction. Once the alveoloplasty will be completed after the elevation of the palatal flap, a third surgical template which is the stackable osteotomy surgical stent will be positioned and mechanically locked to the top of the FG for guided implant placement.
The osteotomy sites will be prepared, through the planned locations and angulations of the surgical guides, using a sequential series of drills of the OGS Surgical Kit After the last drill, six (NeoBiotech Co., Seoul, Korea) implants will be placed freehand after using drill guides, and tightened manually to 35N/cm. Finally, cover screws will be tightened (10 N/cm) to the implants and the surgical guides were removed. The patients will be instructed to complete the course of antibiotic and anti-inflammatory for 5 days after surgery, to maintain good oral hygiene.
Evaluation After the surgery, patients will be submitted to a CBCT scan using the same parameter as the preoperative scan. And the data of the postoperative scan will be superimposed over the preoperative plan to assess the accuracy of the implant placement using the software (blueskybio 4, BlueSky bio, USA). The final actual implant position will be compared to the preoperatively planned position and the deviations will be calculated for global angel deviation and global linear coronal and apical deviation in mm.
- Conditions
- Accuracy of Stackable Guide
- Being tested
- stackable guide
- Keywords
- implant, stackable guide, 3d printing
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
stackable guideDevice
different types of stackable guide
| Study group | Role | What they receive |
|---|---|---|
| selective laser melting (SLM) CO-Cr metal surgical-guides | Active comparator | Not described Receives: Device: stackable guide |
| digital light processing (DLP) resin surgical-guides | Experimental | Not described Receives: Device: stackable guide |
What is being measured
The primary outcome is the main question the study is designed to answer.
global angel deviation and global linear coronal and apical deviation in mm.
patients will be submitted to a CBCT scan using the same parameter as the preoperative scan. And the data of the postoperative scan will be superimposed over the preoperative plan to assess the accuracy of the implant placement using the software (blueskybio 4, BlueSky bio, USA). The final actual implant position will be compared to the preoperatively planned position and the deviations will be calculated for global angel deviation and global linear coronal and apical deviation in mm.
Measured: 1 weekk
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted15 Nov 2022
- Study start5 Oct 2022
- Primary completion25 Dec 2022
- Study completion10 Jan 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Accuracy of Stackable GuideStudies of the same condition, open and under way.
- More trials run by Suez Canal UniversityThe sponsor's other registered studies.
- 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 N/A
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 4 participants (actual)
Sponsor and investigators
- Lead sponsor
- Suez Canal University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05617443
- Sponsor's protocol ID
- 535/2022
- Status last verified
- Nov 2022
- First submitted
- 7 Nov 2022
- Last updated
- 6 May 2023
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 6 May 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparative Assessment For The Positional Accuracy Of Dental Implants Inserted By Computerized Stackable Surgical Guides Made From Selective Laser Melting And Digital Light Processing Technologies
- ClinicalTrials.gov ID
- NCT05617443
- Acronym / sponsor ID
- 535/2022
- Conditions
- Accuracy of Stackable Guide
- Keywords
- implant, stackable guide, 3d printing
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 4 participants (actual)
- Lead sponsor
- Suez Canal UniversityUniversity, hospital or other
- Study start
- 5 Oct 2022 (actual)
- Primary completion
- 25 Dec 2022 (actual)
- Study completion
- 10 Jan 2023 (actual)
- First posted
- 15 Nov 2022 (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.
Purpose; The purpose of this research is to make a comparative estimation for the positional accuracy of dental implants inserted by selective laser melting and digital light processed computerized stackable surgical guides for patients with maxillary terminal dentitions.
Materials and methods; Twenty-four dental implants will be installed in partially edentulous patients who will be applied for treatment of tooth loss and required fixed prosthodontic rehabilitation. Virtually designed prosthetically driven fixation base with its stackable surgical osteotomy guide will be used for bone reduction after tooth extraction and osteotomy preparation respectively. The inserted implants will be divided equally into two groups according to stackable surgical osteotomy guide to either selective laser melting (SLM) CO-Cr metal or digital light processing (DLP) surgical-guides. The final actual implant position will be compared to the preoperative planned position and the deviations will be calculated for coronal deviation, apical deviation in mm, and two angular deviation measurements in degrees.
Detailed description
Preoperative evaluation:
intra-oral and extra-oral examination and medical history for each patient will be recorded to assure that the patient will be eligible for the research.
Written informed consent will be assigned by the patients who will be included in the study.
Preoperative records Polyvinyl siloxane (PVS) impressions for both arches will be made. Also, an interocclusal record will be recorded.
The poured upper and lower cast will be mounted on the articulator and will be scanned using a tabletop scanner (DOF swing, DOF, Korea). the scanned file will be saved in stl format Clinical digital photographs for digital smile design will be used to generate a smile design driven by an individual's face and smile display. As such, it is critical to have at least two portraits representing the lips at rest and another one for a broad smile For each patient, a preoperative cone beam computed tomography (CBCT) scan with the two jaws separated via cotton rolls to separate the volume of interest using a CBCT machine (Scanora 3Dx, Soredex- Finland ) will be taken and saved as Digital Imaging and Communication in Medicine (DICOM) files. The saved STL files will be imported into computer-aided design (CAD) software ( Implastation, prodigident, USA) and superimpose these files to the DICOM files and the JPEG photo files.
Implant and prosthesis planning Virtual tooth setup of the desired prosthetic outcome can be designed to achieve true, restoratively driven implant placement when applied to 3-D surface DICOM data. Performing this virtual wax-up will be done by selecting and importing maxillary teeth from the software library, followed by adjustment of each tooth shape and position according to the patient's occlusion, gender, and smile. The final plan often requires bone reduction to facilitate implant placement and the necessary restorative space for the prosthesis.
A 3-dimensional implant planning using a Software Planning program (Implastation, ProDigident, USA), allows the clinicians to evaluate the osseous tissues concerning the ideal prosthetic position of the virtual waxed-up maxillary teeth. From this information, the sizes and implant receptor sites will be digitally evaluated in all of the necessary views, including cross-sectional, coronal, sagittal, and axial sections followed by virtual placement of the implants.
The stackable guide that will be planned to transfer the virtual plan to the operating field intraorally and consists of 3 components:
- carrier guide: it takes its support from the remaining dentition and has a foundation base attached to it by locks. its function is to transfer the foundation base to its accurate place in the patient mouth.
- foundation base: fixed to bone along the whole surgery time by fixation pins and has locks to be attached with subsequent osteotomy guides.
- osteotomy guide: contains the hole through which the implant drilling will be guided.
The outline of the surgical guide will be determined. and then the thickness and path of insertion. the amount of bone to be reduced will be determined .. a tooth-supported carrier (pin guide) will be designed, it takes its support from the remaining dentition. height of the foundation guide and locations of widely separated 4 anchor pins will be planned so that anchor pins help in achieving the highest degree of surgical accuracy, and then a tooth-supported carrier (pin guide) will be designed, it takes its support from the remaining dentition and accurately replicates the position of the anchor pins for subsequent guides, hence ensuring an accurate replication of the guide position.
With this protocol, teeth removal and bone reduction will be done virtually to provide the available restorative space (from the crest of the bone to the proposed incisal edge position and posterior occlusal plane).
Sleeveless osteotomy guide holes and offset will be designed corresponding to the guided drill kit that will be used(OGS guided kit, oxy implant, Italy) Finally, all guides will be exported as standard triangle language (STL) files and sent to additively manufactured machines.
Grouping:
The inserted implants will be divided equally into two groups according to the stackable surgical osteotomy guide fabrication/printing technique:
First group; in which implants will be placed using selective laser melting (SLM) CO-Cr metal surgical-guides Second group; in which implants will be placed using digital light processing (DLP) resin surgical-guides
Surgical stents fabrication:
For Digital light processing (DLP): DLP printers have a digital projector screen used to flash a single image of each layer on the entire platform at once using curable photopolymer resin. A vat of liquid photopolymer will be exposed to UV light from a digital projector under safelight conditions. The printer (Photon, Anycubic, China) builds the stent one layer at a time by tracing a laser beam on the surface of a vat of printable Resin liquid (SG resin, pro shape, turkey). The process will be repeated, forming another layer on top of the previous layer. This process continues layer by layer until the stent is completed. Printing will be started with a build angle of 45 and the printing thickness on the z-axis was set at 100 microns. After printing, the supports will be removed and the printed stents will be cleaned in an ultrasonic bath with ethyl alcohol for 2 minutes to remove excess resin. Stents will be post-polymerized for 30 minutes using an ultraviolet polymerization unit (bre. Lux power Unit 2, Bredent, Germany).
Regarding Selective Laser Melting (SLM); the STL file will be segmented into cross-sectional layer representations and then exported to a metal laser melting machine (vm120, Vulcan tech, Germany). To fabricate the prototype, this automated printing machine received numerical inputs of the surgical stent design. Sintering of the powder alloy (Starbond easy Pulver 30, Scheftner dental, Germany) to the predesigned guide via high-energy laser beams that traced across a powder bed of densely compacted powdered material, resulting in local melting and fusing of the particles. According to the 3D data fed into the machine, metallic powders will melt together, in a layer-by-layer strategy, creating three-dimensional objects.
Laser spot diameter of 0.08-0.1 mm, sintering speed of 1100-1200 mm/s, a layer thickness of 0.02 mm, and printing angle of 45 degrees, will be considered the parameters of the laser melting machine that will be used for the SLM stent fabrication. SLM stents will be extracted from the base plate and homogenization treatment will be performed at 1150ᵒ C for 30 minutes.
Surgical phase All surgeries will be performed by the same operator under complete aseptic conditions. The patients will be locally anesthetized.
Utilizing the existing dentition to position carrier resin guide to which everything else will be related. Verification of the carrier guide of the pin guide over the teeth will be done.
After verification, the carrier will be securely locked to the foundation metal printed guide and delivered over the teeth. This method allows for the metal foundation guide to be correctly positioned. Four anchor pins will be utilized to stabilize the metal foundation guide (divided equally into anterior and posterior regions bilaterally). An anchoring twist drill will be used with copious irrigation for the preparation of the fixation screw pathway. After that, four anchoring screws will be driven in the anterior and posterior areas After the FG will be secured to the bone, the pin guide will be removed, leaving the maxillary teeth available for extraction. The teeth will be all carefully removed, leaving the remaining alveolus exposed. The outer aspect of the metal FG will be used to determine the amount of bone reduction. Once the alveoloplasty will be completed after the elevation of the palatal flap, a third surgical template which is the stackable osteotomy surgical stent will be positioned and mechanically locked to the top of the FG for guided implant placement.
The osteotomy sites will be prepared, through the planned locations and angulations of the surgical guides, using a sequential series of drills of the OGS Surgical Kit After the last drill, six (NeoBiotech Co., Seoul, Korea) implants will be placed freehand after using drill guides, and tightened manually to 35N/cm. Finally, cover screws will be tightened (10 N/cm) to the implants and the surgical guides were removed. The patients will be instructed to complete the course of antibiotic and anti-inflammatory for 5 days after surgery, to maintain good oral hygiene.
Evaluation After the surgery, patients will be submitted to a CBCT scan using the same parameter as the preoperative scan. And the data of the postoperative scan will be superimposed over the preoperative plan to assess the accuracy of the implant placement using the software (blueskybio 4, BlueSky bio, USA). The final actual implant position will be compared to the preoperatively planned position and the deviations will be calculated for global angel deviation and global linear coronal and apical deviation in mm.
Study design
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| selective laser melting (SLM) CO-Cr metal surgical-guides | Active comparator | Device: stackable guide |
| digital light processing (DLP) resin surgical-guides | Experimental | Device: stackable guide |
Who may qualify
- Ages
- 45 to 75 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- well healthy patients
- patients with maxillary terminal dentition
Key exclusion criteria (3 listed)
- Patients with, systemic disease that might complicate post-operative healing or contribute to bone resorption
- patients with parafunctional habits, poor oral hygiene, limited mouth opening, severe alveolar bone deficiencies,
- patients with uncontrolled diabetes, current irradiation to the head or neck, psychological disorders, or alcohol, tobacco, or drug abuse
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 |
|---|---|---|
| stackable guidedifferent types of stackable guide | Device | digital light processing (DLP) resin surgical-guides, selective laser melting (SLM) CO-Cr metal surgical-guides |
Primary outcome
global angel deviation and global linear coronal and apical deviation in mm.
Time frame: 1 weekk
patients will be submitted to a CBCT scan using the same parameter as the preoperative scan. And the data of the postoperative scan will be superimposed over the preoperative plan to assess the accuracy of the implant placement using the software (blueskybio 4, BlueSky bio, USA). The final actual implant position will be compared to the preoperatively planned position and the deviations will be calculated for global angel deviation and global linear coronal and apical deviation in mm.
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 6 May 2023.
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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 study testing stackable guide in people with Accuracy of Stackable Guide, run by Suez Canal University at 1 site in Egypt.
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 2 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 6 May 2023. 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 Egypt. 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.
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?
global angel deviation and global linear coronal and apical deviation in mm. (time frame: 1 weekk). 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 6 May 2023.