Superficial Basal Cell CarcinomaPhase 4NCT01491711
Superficial Basal Cell Carcinoma Treatment With Topical Photodynamic Therapy With Fractionated 5-aminolevulinic Acid 20% Versus Two Stage Methylaminolevulinate
A Phase 4 study testing Methylaminolevulinate PDT in 2 sessions and Fractionated 5-aminolevulinic acid hydrochloride 20% gel PDT in people with Superficial Basal Cell Carcinoma, run by Maastricht University Medical Center at 3 sites in Netherlands.
Trial summary
Skin cancer is the most common cancer in Caucasians, and a basal cell carcinoma (BCC) being the most common skin cancer with around 44,000 new tumours per year, and its incidence is still rising. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Superficial Basal Cell Carcinoma
- What is being tested?
- Methylaminolevulinate PDT in 2 sessions and Fractionated 5-aminolevulinic acid hydrochloride 20% gel PDT
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 162 participants
- Where
- 3 sitesNetherlands
- Study dates
- Aug 2013to Apr 2015
- 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 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Minimal age of 18 years
- Histological proven BCC
- Primary BCC (no previous treatment)
- Being able to understand instructions
Who cannot join
- Age under 18 years
- No histological proven BCC
- Recurrent BCC (previously treated)
- Not able to understand instructions
- Concomitant disease requiring systematic immunosuppressive treatment
- Genetic skin cancer disorders
Trial locations and contacts
3 sites in 1 country.
Netherlands3 sites, 3 recruiting
- Recruiting
Maastricht University Medical Center
Maastricht, Limburg, 6202 AZ
N WJ Kelleners-Smeets, MD, PhD, 0031433877295, n.kelleners.smeets@mumc.nl
J JPHM Kessels, MD, 0031433877295, janneke.kessels@mumc.nl
- Recruiting
Erasmus Medical Centre
Rotterdam, South Holland, 3015 CE
E RM de Haas, MD, PhD, 0031107034849, e.r.m.dehaas@erasmusmc.nl
H Kreukels, MD, 0031107040110, h.kreukels@erasmusmc.nl
- Recruiting
VieCuri Medical Centre
Venlo, Limburg, 5912 BL
J PA van Pelt, MD, PhD
M JM van Rooij, MD, PhD
About this study
Official title: Treatment of Superficial Basal Cell Carcinoma by Topical Photodynamic Therapy With Fractionated 5-aminolevulinic Acid 20% Versus Two Stage Topical Photodynamic Therapy With Methylaminolevulinate
Skin cancer is the most common cancer in Caucasians, and a basal cell carcinoma (BCC) being the most common skin cancer with around 44,000 new tumours per year, and its incidence is still rising. In the past it has been a disease of the elderly patient but as a consequence of recreational sun exposure and tanning beds, more young patients develop a skin cancer as well. There are different subtypes of BCC and most subtypes are treated by surgical excision. Nowadays, non-invasive techniques as photodynamic therapy (PDT) are common practice to treat superficial BCC (sBCC). Because of these techniques treatment by surgical excision can be avoided with the possibility of complications and scar formation. Both 5-aminolevulino acid (5-ALA) and the more lipophilic methyl aminolevulinate (MAL) can be used as a precursor of the photosensitiser. These agents generate an excess of protoporphyrin IX in metabolic active cells, which are illuminated by a specific light source leading to release of reactive oxygen radicals in tissue. The result is apoptosis and necrosis of tumour cells. At the moment, two treatment protocols are used in the Netherlands: the fractionated 5-ALA 20% (Fagron) protocol according to de Haas and the MAL (Metvix, Galderma) protocol. Because MAL was first marketed and registered as a treatment option for premalignant and superficial malignancies most hospitals in the Netherlands use this topical agent. However, there is no evidence which of the 2 agents is more (cost-)effective and/ or preferred by patients.
Objective: to determine which treatment is the most effective treatment in terms of prevention of treatment failure, cost saving and patients preference when comparing fractionated 5-ALA 20% PDT versus MAL PDT in 2 treatment sessions.
Read the detailed description
- Basal cell carcinoma throughout the world
Skin cancer is the most common form of cancer, with basal cell carcinoma (BCC) being the most common form of all skin cancers, and the incidence is still rising.1,2 Of all types of BCC, superficial basal cell carcinoma (sBCC), is the histopathologic subtype with the fastest growing incidence, especially on the trunk in younger patients.3-5 It is a common health problem and although there is no chance of metastasis it can lead to more aggressive forms of BCC with the ability to cause serious local destruction.
- Treatment options
The DBC (diagnose behandel combinatie) cost price, the amount received for diagnostic and treatment of one BCC, for surgical excision is partly free negotiable between each hospital and health insurances. Only the DBC cost price of patients whose health insurance has no contract with the hospital is public for everyone. This leads to around 18 million euro (based on a cost price of 400.00 euro for 44,000 new BCCs per year) that is yearly spent on the surgical treatment of BCC in the Netherlands and cost will only increase in future with the growing incidence.6 For most BCC subtypes the only effective treatment is surgery but for sBCC other non-invasive treatments like photodynamic therapy (PDT) are suitable. It is well accepted in today's dermatologic practice that surgical excision can be considered as over-treatment for sBCC.7-9 PDT is superior to surgical excision in primary sBCC of any size in low-risk sites.9 As a consequence unnecessary anaesthesia and incisions are avoided thereby preventing side-effects, such as scars, haematomas or functional disruption, and healthy tissue is preserved. MAL is a worldwide registered agent for the use of topical PDT in sBCC while 5-ALA is not registered in the European Union. In the Netherlands both fractionated 5-ALA 20% and MAL PDT in 2 sessions are used as treatment for sBCC. Although there are studies showing the effectiveness of both treatment regimens, the effectiveness, costs and patient preferences have never been studied in a prospective randomised trial.
- Developments in treatment: photodynamic therapy
PDT has become increasingly implemented in standard care for sBCC in the last years.8-10 Nowadays, in the Maastricht University Medical Centre, about 60% of patients are treated with PDT. Similar situations are found in the Erasmus MC Rotterdam and the VieCuri Medical Centre Venlo/Venray. On national level, around two thirds of patients are treated with MAL PDT in 2 sessions and one third with fractionated 5-ALA 20% PDT. This distribution is historically determined and not based on evidence based research.
- 5-ALA 20% PDT versus MAL PDT
There are only a few randomised controlled studies on treatment of the most common skin cancer.11 Choice of PDT treatment with fractionated 5-ALA 20% or MAL in 2 sessions often depends on the experience and choice of the physician or the availability of the precursor in a hospital. World-wide, most studies are performed with MAL and it has been accepted as the standard of care in PDT.12 However, according to the literature, the effectiveness in terms of clearance rates is in different studies lower for MAL in two sessions compared to fractionated 5-ALA 20% PDT: 79% versus 97% intention to treat (ITT) after one year in sBCC.13,14 Contra dictionary, MAL has the theoretical benefit of being more and faster absorbed in the cell than 5-ALA 20% and, thereby, should generate a higher production of protoporphyrin IX. In addition MAL has higher selectivity for tumour cells, inducing fewer side-effects in normal tissue. 15,16 This discrepancy between theoretical working mechanism and clearance rates needs further clinical research of the effectiveness of both treatments.
PDT is a hospital administered treatment modality during which patients have to come to the hospital one day (fractionated 5-ALA 20%) or two days one week apart (MAL in 2 sessions). Patient compliance could be higher with fractionated 5-ALA 20% than with MAL in 2 sessions because patients have to visit the hospital a second time. At some parts of the body patients experience a variable burning pain sensation during PDT which might influence completing the treatment. Kuijpers et al. found no significant differences in pain scores between ALA-PDT in 2 sessions and MAL PDT in 2 sessions.17 We expect 5-ALA 20% PDT to have more side-effects in our study as patients are treated twice on the same day.
Furthermore it is important to take into consideration the differences in patient acceptability costs (see 'economic evaluation').18 A well-designed study comparing the two topical PDT treatment modalities: fractionated 5-ALA 20% and MAL in 2 sessions will provide the answers needed to establish the position of the two modalities in the treatment of patients with sBCC. The conclusions from the proposed study can serve as a basis for updating guidelines for the treatment of sBCC to catch up with recent developments in clinical practice.
- Conditions
- Superficial Basal Cell Carcinoma
- Being tested
- Methylaminolevulinate PDT in 2 sessions, Fractionated 5-aminolevulinic acid hydrochloride 20% gel PDT
- Keywords
- Superficial basal cell carcinoma, Carcinoma, Basal Cell, Skin diseases, Connective tissue diseases, Treatment, Drug therapy, Efficacy, Photodynamic therapy, Photosensitizing Agents/therapeutic use, Aminolevulinic acid, Methylaminolevulinate, Pain measurement, Health Care Economics and Organizations
- Medical subject headings
- Carcinoma, Basal Cell, Skin Diseases, Connective Tissue Diseases
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Methylaminolevulinate PDT in 2 sessionsDrug
Also called Metvix 160 mg/g creme, CAS number 33320-16-0, ATC code L01XD03, RVG 31130
The methylaminolevulinate creme is applied to the tumour with a margin of 1 cm, ± 1-2 mm thick. Tegaderm®, a gauze and tinfoil is placed over the area to prevent contact with UV light. After 4 hours the area is illuminated with Aktilite (632 nm, 570-670 nm, 75 J/cm2). The light intensity at the lesion surface should not exceed 200 mW/cm2. During illumination a fan is used to cool the treatment site. After the first treatment the skin area is covered to prevent exposure to daylight during 48 hours. After one week (on day 8), the same procedure is repeated. After the treatment the skin area is covered to prevent exposure to daylight during 48 hours. A side-effect of the treatment is a burning pain during illumination and slight erythema afterwards lasting a few days. Sometimes blistering occurs.
Fractionated 5-aminolevulinic acid hydrochloride 20% gel PDTDrug
The 5-ALA HCl 20% gel is applied to the tumour with a margin of 1 cm, ± 1-2 mm thick. Tegaderm®, a gauze and tinfoil is placed over the area to prevent contact with UV light. After 4 hours the area is illuminated with Aktilite (632 nm). During illumination a fan is used to cool the treatment site. The treatment site is covered again with Tegaderm for 2 hours after first treatment, whereupon a second illumination with the same light takes place. A side-effect of the treatment is a burning pain during illumination and slight erythema afterwards lasting a few days. Sometimes blistering occurs. Patients are advised to avoid direct sunlight two days after treatment.
| Study group | Role | What they receive |
|---|---|---|
| Fractionated 5-ALA HCl 20% gel PDT | Active comparator | Twice on day 1 Receives: Drug: Fractionated 5-aminolevulinic acid hydrochloride 20% gel PDT |
| Methylaminolevulinate PDT in 2 sessions | Active comparator | On day 1 and 8 Receives: Drug: Methylaminolevulinate PDT in 2 sessions |
What is being measured
The primary outcome is the main question the study is designed to answer.
Treatment failure
Histological proven treatment failure one year after treatment of sBCC with fractionated 5-ALA 20% PDT versus MAL PDT in 2 sessions. If there is any clinical suspicion of residual tumour at control visits 3 and 12 months posttreatment, a 3 mm punch biopsy will be taken to confirm the diagnosis by histopathology.
Measured: 12 months posttreatment
Secondary outcomes (2)
Patient preferences
Patient preferences of treatment with fractionated 5-ALA 20% PDT versus MAL PDT in 2 sessions.
A patient questionnaire will be given twice: on last day of treatment and 1 week posttreatment
Measured: 1 week posttreatment
Health care costs
Health care costs of treatment with fractionated 5-ALA 20% PDT versus MAL PDT in 2 sessions.
Measured: 12 months posttreatment
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted14 Dec 2011 (estimated)
- Study startAug 2013
- Primary completionApr 2015 (estimated)
- Study completionApr 2015 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Superficial Basal Cell CarcinomaStudies of the same condition, open and under way.
- More trials run by Maastricht University Medical CenterThe 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 4
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Investigator
- Enrolment
- 162 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Maastricht University Medical Center
- Sponsor type
- University, hospital or other
- Collaborators
- Erasmus Medical Center, VieCuri Medical Centre
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01491711
- Sponsor's protocol ID
- NL38127
- Status last verified
- Jan 2014
- First submitted
- 5 Dec 2011
- Last updated
- 31 Jan 2014
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 31 Jan 2014. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Treatment of Superficial Basal Cell Carcinoma by Topical Photodynamic Therapy With Fractionated 5-aminolevulinic Acid 20% Versus Two Stage Topical Photodynamic Therapy With Methylaminolevulinate
- ClinicalTrials.gov ID
- NCT01491711
- Acronym / sponsor ID
- NL38127
- Conditions
- Superficial Basal Cell Carcinoma
- Keywords
- Superficial basal cell carcinoma, Carcinoma, Basal Cell, Skin diseases, Connective tissue diseases, Treatment, Drug therapy, Efficacy, Photodynamic therapy
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 162 participants (estimated)
- Lead sponsor
- Maastricht University Medical CenterUniversity, hospital or other
- Collaborators
- Erasmus Medical Center, VieCuri Medical Centre
- Study start
- Aug 2013
- Primary completion
- Apr 2015 (estimated)
- Study completion
- Apr 2015 (estimated)
- First posted
- 14 Dec 2011 (estimated)
- 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.
Skin cancer is the most common cancer in Caucasians, and a basal cell carcinoma (BCC) being the most common skin cancer with around 44,000 new tumours per year, and its incidence is still rising. In the past it has been a disease of the elderly patient but as a consequence of recreational sun exposure and tanning beds, more young patients develop a skin cancer as well. There are different subtypes of BCC and most subtypes are treated by surgical excision. Nowadays, non-invasive techniques as photodynamic therapy (PDT) are common practice to treat superficial BCC (sBCC). Because of these techniques treatment by surgical excision can be avoided with the possibility of complications and scar formation. Both 5-aminolevulino acid (5-ALA) and the more lipophilic methyl aminolevulinate (MAL) can be used as a precursor of the photosensitiser. These agents generate an excess of protoporphyrin IX in metabolic active cells, which are illuminated by a specific light source leading to release of reactive oxygen radicals in tissue. The result is apoptosis and necrosis of tumour cells. At the moment, two treatment protocols are used in the Netherlands: the fractionated 5-ALA 20% (Fagron) protocol according to de Haas and the MAL (Metvix, Galderma) protocol. Because MAL was first marketed and registered as a treatment option for premalignant and superficial malignancies most hospitals in the Netherlands use this topical agent. However, there is no evidence which of the 2 agents is more (cost-)effective and/ or preferred by patients.
Objective: to determine which treatment is the most effective treatment in terms of prevention of treatment failure, cost saving and patients preference when comparing fractionated 5-ALA 20% PDT versus MAL PDT in 2 treatment sessions.
Detailed description
- Basal cell carcinoma throughout the world
Skin cancer is the most common form of cancer, with basal cell carcinoma (BCC) being the most common form of all skin cancers, and the incidence is still rising.1,2 Of all types of BCC, superficial basal cell carcinoma (sBCC), is the histopathologic subtype with the fastest growing incidence, especially on the trunk in younger patients.3-5 It is a common health problem and although there is no chance of metastasis it can lead to more aggressive forms of BCC with the ability to cause serious local destruction.
- Treatment options
The DBC (diagnose behandel combinatie) cost price, the amount received for diagnostic and treatment of one BCC, for surgical excision is partly free negotiable between each hospital and health insurances. Only the DBC cost price of patients whose health insurance has no contract with the hospital is public for everyone. This leads to around 18 million euro (based on a cost price of 400.00 euro for 44,000 new BCCs per year) that is yearly spent on the surgical treatment of BCC in the Netherlands and cost will only increase in future with the growing incidence.6 For most BCC subtypes the only effective treatment is surgery but for sBCC other non-invasive treatments like photodynamic therapy (PDT) are suitable. It is well accepted in today's dermatologic practice that surgical excision can be considered as over-treatment for sBCC.7-9 PDT is superior to surgical excision in primary sBCC of any size in low-risk sites.9 As a consequence unnecessary anaesthesia and incisions are avoided thereby preventing side-effects, such as scars, haematomas or functional disruption, and healthy tissue is preserved. MAL is a worldwide registered agent for the use of topical PDT in sBCC while 5-ALA is not registered in the European Union. In the Netherlands both fractionated 5-ALA 20% and MAL PDT in 2 sessions are used as treatment for sBCC. Although there are studies showing the effectiveness of both treatment regimens, the effectiveness, costs and patient preferences have never been studied in a prospective randomised trial.
- Developments in treatment: photodynamic therapy
PDT has become increasingly implemented in standard care for sBCC in the last years.8-10 Nowadays, in the Maastricht University Medical Centre, about 60% of patients are treated with PDT. Similar situations are found in the Erasmus MC Rotterdam and the VieCuri Medical Centre Venlo/Venray. On national level, around two thirds of patients are treated with MAL PDT in 2 sessions and one third with fractionated 5-ALA 20% PDT. This distribution is historically determined and not based on evidence based research.
- 5-ALA 20% PDT versus MAL PDT
There are only a few randomised controlled studies on treatment of the most common skin cancer.11 Choice of PDT treatment with fractionated 5-ALA 20% or MAL in 2 sessions often depends on the experience and choice of the physician or the availability of the precursor in a hospital. World-wide, most studies are performed with MAL and it has been accepted as the standard of care in PDT.12 However, according to the literature, the effectiveness in terms of clearance rates is in different studies lower for MAL in two sessions compared to fractionated 5-ALA 20% PDT: 79% versus 97% intention to treat (ITT) after one year in sBCC.13,14 Contra dictionary, MAL has the theoretical benefit of being more and faster absorbed in the cell than 5-ALA 20% and, thereby, should generate a higher production of protoporphyrin IX. In addition MAL has higher selectivity for tumour cells, inducing fewer side-effects in normal tissue. 15,16 This discrepancy between theoretical working mechanism and clearance rates needs further clinical research of the effectiveness of both treatments.
PDT is a hospital administered treatment modality during which patients have to come to the hospital one day (fractionated 5-ALA 20%) or two days one week apart (MAL in 2 sessions). Patient compliance could be higher with fractionated 5-ALA 20% than with MAL in 2 sessions because patients have to visit the hospital a second time. At some parts of the body patients experience a variable burning pain sensation during PDT which might influence completing the treatment. Kuijpers et al. found no significant differences in pain scores between ALA-PDT in 2 sessions and MAL PDT in 2 sessions.17 We expect 5-ALA 20% PDT to have more side-effects in our study as patients are treated twice on the same day.
Furthermore it is important to take into consideration the differences in patient acceptability costs (see 'economic evaluation').18 A well-designed study comparing the two topical PDT treatment modalities: fractionated 5-ALA 20% and MAL in 2 sessions will provide the answers needed to establish the position of the two modalities in the treatment of patients with sBCC. The conclusions from the proposed study can serve as a basis for updating guidelines for the treatment of sBCC to catch up with recent developments in clinical practice.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (investigator)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Fractionated 5-ALA HCl 20% gel PDT | Active comparator | Drug: Fractionated 5-aminolevulinic acid hydrochloride 20% gel PDTTwice on day 1 |
| Methylaminolevulinate PDT in 2 sessions | Active comparator | Drug: Methylaminolevulinate PDT in 2 sessionsOn day 1 and 8 |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Minimal age of 18 years
- Histological proven BCC
- Primary BCC (no previous treatment)
- Being able to understand instructions
Key exclusion criteria (6 listed)
- Age under 18 years
- No histological proven BCC
- Recurrent BCC (previously treated)
- Not able to understand instructions
- Concomitant disease requiring systematic immunosuppressive treatment
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 |
|---|---|---|
| Methylaminolevulinate PDT in 2 sessionsAlso: Metvix 160 mg/g creme, CAS number 33320-16-0, ATC code L01XD03, RVG 31130The methylaminolevulinate creme is applied to the tumour with a margin of 1 cm, ± 1-2 mm thick. Tegaderm®, a gauze and tinfoil is placed over the area to prevent contact with UV light. After 4 hours the area is illuminated with Aktilite (632 nm, 570-670 nm, 75 J/cm2). The light intensity at the lesion surface should not exceed 200 mW/cm2. During illumination a fan is used to cool the treatment site. After the first treatment the skin area is covered to prevent exposure to daylight during 48 hours. After one week (on day 8), the same procedure is repeated. After the treatment the skin area is covered to prevent exposure to daylight during 48 hours. A side-effect of the treatment is a burning pain during illumination and slight erythema afterwards lasting a few days. Sometimes blistering occurs. | Drug | Methylaminolevulinate PDT in 2 sessions |
| Fractionated 5-aminolevulinic acid hydrochloride 20% gel PDTThe 5-ALA HCl 20% gel is applied to the tumour with a margin of 1 cm, ± 1-2 mm thick. Tegaderm®, a gauze and tinfoil is placed over the area to prevent contact with UV light. After 4 hours the area is illuminated with Aktilite (632 nm). During illumination a fan is used to cool the treatment site. The treatment site is covered again with Tegaderm for 2 hours after first treatment, whereupon a second illumination with the same light takes place. A side-effect of the treatment is a burning pain during illumination and slight erythema afterwards lasting a few days. Sometimes blistering occurs. Patients are advised to avoid direct sunlight two days after treatment. | Drug | Fractionated 5-ALA HCl 20% gel PDT |
Primary outcome
Treatment failure
Time frame: 12 months posttreatment
Histological proven treatment failure one year after treatment of sBCC with fractionated 5-ALA 20% PDT versus MAL PDT in 2 sessions. If there is any clinical suspicion of residual tumour at control visits 3 and 12 months posttreatment, a 3 mm punch biopsy will be taken to confirm the diagnosis by histopathology.
2 secondary outcomes
Patient preferences
Time frame: 1 week posttreatment
Health care costs
Time frame: 12 months posttreatment
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 31 Jan 2014.
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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.
3 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing Methylaminolevulinate PDT in 2 sessions and Fractionated 5-aminolevulinic acid hydrochloride 20% gel PDT in people with Superficial Basal Cell Carcinoma, run by Maastricht University Medical Center at 3 sites in Netherlands.
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 4 inclusion and 6 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: status not confirmed, as of the sponsor's last update on 31 Jan 2014. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 3 sites in Netherlands. 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?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Nicole WJ Kelleners-Smeets, MD, PhD (0031433877295, n.kelleners.smeets@mumc.nl), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Treatment failure (time frame: 12 months posttreatment). 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 31 Jan 2014.