Breast FibroadenomaPhase 2NCT03715413
Analgesic Efficacy of Pulsed Radiofrequency in Non-cyclic Mastalgia
A Phase 2 study testing pulsed radiofrequency of 2nd , 3rd and 4th thoracic dorsal root ganglia. and Tamoxifen in people with Breast Fibroadenoma, run by Mansoura University at 1 site in Egypt.
Trial summary
Background: Breast pain, mastalgia or mastodynia, is recognized as an organic benign breast disease. Mastalgia may be bilateral, may be in only one breast or part of one breast, and may radiate to the axilla and down the medial aspect of the upper arm. Read more about this study
- Who is it for?
- Ages 20 to 60 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Breast Fibroadenoma
- What is being tested?
- pulsed radiofrequency of 2nd , 3rd and 4th thoracic dorsal root ganglia. and Tamoxifen
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 64 participants
- Where
- 1 siteEgypt
- Study dates
- 15 Aug 2018to 1 Dec 2018
- Phase
- Phase 2
- 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 20 to 60 years
- Women only
- Healthy volunteers accepted
- Adult
Who may be able to join
- complain from non-cyclic mastalgia aged from 20 to 60 with VAS > 4
Who cannot join
- cyclical mastalgia
- extra-mammary mastalgia
- patients refusal
- suspicion of malignancy
- acute inflammatory breast conditions
- presence of polycystic ovarian diseases or cervical hyperplasia
Show all 12Show fewer
- pregnant patients and patients during lactation period
- coagulopathy disorder
- sepsis at the side of injection
- history of thromboembolic disease
- mental disorder and who was not willing or cannot finish the whole study
- disturbed anatomy (congenital, traumatic, and postsurgical), which increase the intervention difficulty.
Trial locations and contacts
1 site in 1 country.
About this study
Background: Breast pain, mastalgia or mastodynia, is recognized as an organic benign breast disease. Mastalgia may be bilateral, may be in only one breast or part of one breast, and may radiate to the axilla and down the medial aspect of the upper arm. This study aimed to evaluate the additional pulsed radiofrequency of 2nd , 3rd and 4th thoracic dorsal root ganglia to the routine regimen treatment of mastalgia tamoxifen 10 mg daily may improve breast pain severity and quality of life.
Method: Patients was randomly classified into two groups:Group A (n=13): they was received Tamoxifen 10 mg daily. Group B (n=13): they was received Tamoxifen 10 mg daily and pulsed radiofrequency of 2nd , 3rd and 4th thoracic dorsal root ganglia. The following parameters were monitored: Primary outcome: VAS after injection and at interval two weeks, 1, 2 and 3 months after injection. Secondary outcome:1-Immediate complications for ex. Hematoma, neurological deficits or respiratory insufficiency (dyspnea or pneumothorax).2-Need for analgesic intake was recorded.3-Side effect of Tamoxifen as nausea, vomiting, hot flashes and dizziness.4-Quality of life (The American Chronic Pain Association's Quality of life scale).
Read the detailed description
Introduction:
Breast pain, mastalgia or mastodynia, is recognized as an organic benign breast disease . It can be severe enough to cause disturbances in normal quality of life rating which leads to disorders in sexual, physical, and social activities. When compared with other conditions, it will be similar to chronic cancer pain in the mean pain-index .
Breast pain is classified into three main categories: cyclical, non-cyclical and extra-mammary mastalgia. Cyclical pain is the commonest and it has a temporal association with the menstrual cycle. Pain characteristically starts in the days before menstruation and gradually increases. It tends to subside once menstruation has started and often disappears after a few days. Pain in these women usually abates after the menopause. These factors suggest a hormonal aetiology, high level of estrogen, low level of progesterone, and imbalance in estrogen to progesterone ratio are assumed among its causes, as well. Furthermore, many women associate the onset and resolution of cyclical mastalgia with a hormonal event, such as pregnancy or taking the oral contraceptive pill .
In contrast, there is no relationship to the menstrual cycle with non-cyclical mastalgia. Non-cyclic breast pain may result from pregnancy, mastitis, trauma, thrombophlebitis, macrocysts, psychologic disturbance, benign tumors, or cancer. However, only a minority of breast pain is explained by these conditions. Most non-cyclic breast pain arises for unknown reasons. Typically, it presents at a later age; most women are in the fourth or fifth decade of life at diagnosis. Many women are postmenopausal at onset of symptoms. Unfortunately, the course of both cyclical and non-cyclical mastalgia may be long and last many years.
The origin of extra-mammary pain is variable. Referred pain from cardiac, pulmonary and gastrointestinal causes, such as angina, pneumonia and oesophagitis, respectively, need to be excluded. A common cause of extra-mammary mastalgia arises from inflammation of the costochondral junctions of the chest wall (Tietze's disease). This condition usually resolves with rest and non-steroidal anti-inflammatory drugs .
Mastalgia may be bilateral, may be in only one breast or part of one breast, and may radiate to the axilla and down the medial aspect of the upper arm. The affected breast is often extremely tender to touch and pain may be accompanied by swelling and congestion.
A variety of medical therapies such as non-steroidal anti-inflammatory drugs (NSAIDs), vitamin B2, B6, E and C, diuretics, progesterone, thyroxin, Tamoxifen, Bromocriptine, Danazol, and plant extracts like evening primrose oil (EPO) and vitexagnus castus have been recommended for treatment of mastalgia. Unfortunately, Non-cyclic mastalgia responds poorly to medical treatment.
Psychological reassurance and active life style play a role to decrease the pain and low-fat, high-carbohydrate diet can also effect an improvement.
the female breast supplied its innervation from the anterior and lateral cutaneous branches of the second to the sixth intercostal nerves .
Tamoxifen is one of the medical treatment of mastalgia and considered as a first medication line. Tamoxifen 10 mg daily is effective in the treatment of mastalgia. It has side effects commonly observed in short-term treatment as weight gain, nausea, hot flashes (10%), bloating (5% or less), menstrual irregularity, amenorrhea (10%) and vaginal dryness. Thromboembolic is a rare but serious side effects of tamoxifen so it is contraindicated in women with a history of thromboembolic disease.
Pulsed radiofrequency (PRF) has recently been developed with widely usage by pain practitioners as alternative therapeutic technique for relief of chronic pain .
In our study, the investigators aim that the additional pulsed radiofrequency of 2nd , 3rd and 4th thoracic dorsal root ganglia to the routine regimen treatment of mastalgia tamoxifen 10 mg daily may improve breast pain severity and quality of life.
Our proposal: Is to find that pulsed radiofrequency of 2nd , 3rd and 4th thoracic dorsal root ganglia may improve breast pain severity and quality of life.
Aim of the work: This study aimed to evaluate the efficacy of additional pulsed radiofrequency (2nd , 3rd and 4th thoracic dorsal root ganglia) to the routine regimen treatment of mastalgia tamoxifen 10 mg daily.
Hypothesis: Management of non cyclic mastalgia is a challenging issue needing more appropriate method to reach the best result.
Recharge Gap: To our knowledge, there is a no researches discuss this issue and how to manage it in best way.
Patients and methods:
After approval of the local ethics committee (Mansoura university), twenty six patients complain from non-cyclic mastalgia aged from 18 to 60 with VAS > 4 was enrolled in this prospective study who were recruited from outpatient pain clinic in Oncology Center Mansoura University.
Sample size:
It was assessed using G-power analysis. Assuming α (type I error) = 0.05 and β (type II error) = 0.2 (power = 80 %) and effect size (δ) = 0.6 yielded a total sample size of 26.
Patients was randomly classified into two groups:
Group A (n=13): they was received Tamoxifen 10 mg daily. Group B (n=13): they was received Tamoxifen 10 mg daily and pulsed radiofrequency of 2nd , 3rd and 4th thoracic dorsal root ganglia.
Exclusion criteria: cyclical mastalgia, extra-mammary mastalgia patients refusal, suspicion of malignancy, acute inflammatory breast conditions, presence of polycystic ovarian diseases or cervical hyperplasia, pregnant patients and patients during lactation period, coagulopathy disorder, sepsis at the side of injection, history of thromboembolic disease, mental disorder and who was not willing or cannot finish the whole study, disturbed anatomy (congenital, traumatic, and postsurgical), which increase the intervention difficulty.
All patients in group B will inform about the procedure and its possible consequences. Written informed consent was obtained from all patients before the procedure.
Technique:
An intravenous cannula was inserted and secured. All suitable resuscitation equipment and drugs will available. Vital signs, heart rate, blood pressure and oxygen saturation will monitored throughout the procedure and up to 1 hour after the block performance.
Resuscitation equipment must be readily available including endotracheal tubes of different sizes, ambu bag, ventilator, druges eg. atropine and adrenaline.
The procedures were performed on a 64 MDCT scanner (Brilliance 64-Philips). The CT acquisition parameters were 200 mAs, 120 kVp, 512 × 512 matrix, 1.172 pitches, 64 × 0.625 mm section collimation, and 4 mm slice thickness.
Patients were lying prone. First, a level of T2, 3, 4 disc was detected then the target 2nd, 3rd and 4th thoracic nerve roots were identified. After marking the entry points, adequate sterilization of the skin was achieved using bovidone iodine then the skin was anasthesied by 2 ml lidocaine 2% at each entry point. The Baileys radio frequency (RF) 22G, 10 cm, sharp needles with 10 mm active tip was introduced to face the 2nd, 3rd and 4th thoracic nerve roots. If the lung or the pleura are within the needle path injection of saline in order to push the lung or the pleura away from the field.
When confirm the place of the needles tips, the sensory and motor stimulations were done by the RF generator to get sensory paresthesia along T2, T3 and T4 dermatomes at 0.4-0.8 V and intercostal fasciculation were obtained at double the sensory amplitude.
The PRF course was carried out at 42°C for 120 s twice at each level followed by injection of 1 ml lidocaine 2% and 1 ml dexamethasone 4 mg at each level.
After intervention, All patients were transferred to a recovery room for observation and record any complication.
- Conditions
- Breast Fibroadenoma
- Being tested
- pulsed radiofrequency of 2nd , 3rd and 4th thoracic dorsal root ganglia., Tamoxifen
- Keywords
- pulsed radiofrequency, non-cyclic mastalgia
- Medical subject headings
- Fibroadenoma
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
pulsed radiofrequency of 2nd , 3rd and 4th thoracic dorsal root ganglia.Other
Patients were lying prone. Firstly, T2, 3, 4 disc level was detected then the target 2nd, 3rd and 4th thoracic nerve roots were identified. After marking the entry points, adequate sterilization of the skin was achieved using bovidone iodine then the skin was anasthesied by 2 ml lidocaine 2% at each entry point. The Baileys radio frequency (RF) 22G, 10 cm, sharp needles with 10 mm active tip was introduced to face the 2nd, 3rd and 4th thoracic nerve roots.The PRF course was carried out at 42°C for 120 s twice at each level followed by injection of 1 ml lidocaine 2% and 1 ml dexamethasone 4 mg at each level.
TamoxifenDrug
received Tamoxifen 10 mg daily
| Study group | Role | What they receive |
|---|---|---|
| Tamoxifen group | Other | they was received Tamoxifen 10 mg daily. Receives: Drug: Tamoxifen |
| Tamoxifen and pulsed radiofrequency group | Active comparator | they was received Tamoxifen 10 mg daily and pulsed radiofrequency of 2nd , 3rd and 4th thoracic dorsal root ganglia. Receives: Other: pulsed radiofrequency of 2nd , 3rd and 4th thoracic dorsal root ganglia.; Drug: Tamoxifen |
What is being measured
The primary outcome is the main question the study is designed to answer.
VAS
0=no pain, 10=worst pain
Measured: 3 months
Secondary outcomes (2)
Immediate complications for ex
Hematoma, neurological deficits or respiratory insufficiency (dyspnea or pneumothorax).
Measured: one day
Side effect of Tamoxifen
nausea, vomiting, hot flashes and dizziness.
Measured: 3 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 Oct 2018
- Study start15 Aug 2018
- Primary completion1 Dec 2018
- Study completion1 Dec 2018
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Breast FibroadenomaStudies of the same condition, open and under way.
- More trials run by Mansoura 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 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 64 participants (actual)
Sponsor and investigators
- Lead sponsor
- Mansoura University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Nevert Adel, Mansoura University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03715413
- Sponsor's protocol ID
- MansouraU3
- Status last verified
- Mar 2019
- First submitted
- 15 Oct 2018
- Last updated
- 7 Mar 2019
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 7 Mar 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Analgesic Efficacy of Pulsed Radiofrequency in Non-cyclic Mastalgia
- ClinicalTrials.gov ID
- NCT03715413
- Acronym / sponsor ID
- MansouraU3
- Conditions
- Breast Fibroadenoma
- Keywords
- pulsed radiofrequency, non-cyclic mastalgia
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 64 participants (actual)
- Lead sponsor
- Mansoura UniversityUniversity, hospital or other
- Study start
- 15 Aug 2018 (actual)
- Primary completion
- 1 Dec 2018 (actual)
- Study completion
- 1 Dec 2018 (actual)
- First posted
- 23 Oct 2018 (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.
Background: Breast pain, mastalgia or mastodynia, is recognized as an organic benign breast disease. Mastalgia may be bilateral, may be in only one breast or part of one breast, and may radiate to the axilla and down the medial aspect of the upper arm. This study aimed to evaluate the additional pulsed radiofrequency of 2nd , 3rd and 4th thoracic dorsal root ganglia to the routine regimen treatment of mastalgia tamoxifen 10 mg daily may improve breast pain severity and quality of life.
Method: Patients was randomly classified into two groups:Group A (n=13): they was received Tamoxifen 10 mg daily. Group B (n=13): they was received Tamoxifen 10 mg daily and pulsed radiofrequency of 2nd , 3rd and 4th thoracic dorsal root ganglia. The following parameters were monitored: Primary outcome: VAS after injection and at interval two weeks, 1, 2 and 3 months after injection. Secondary outcome:1-Immediate complications for ex. Hematoma, neurological deficits or respiratory insufficiency (dyspnea or pneumothorax).2-Need for analgesic intake was recorded.3-Side effect of Tamoxifen as nausea, vomiting, hot flashes and dizziness.4-Quality of life (The American Chronic Pain Association's Quality of life scale).
Detailed description
Introduction:
Breast pain, mastalgia or mastodynia, is recognized as an organic benign breast disease . It can be severe enough to cause disturbances in normal quality of life rating which leads to disorders in sexual, physical, and social activities. When compared with other conditions, it will be similar to chronic cancer pain in the mean pain-index .
Breast pain is classified into three main categories: cyclical, non-cyclical and extra-mammary mastalgia. Cyclical pain is the commonest and it has a temporal association with the menstrual cycle. Pain characteristically starts in the days before menstruation and gradually increases. It tends to subside once menstruation has started and often disappears after a few days. Pain in these women usually abates after the menopause. These factors suggest a hormonal aetiology, high level of estrogen, low level of progesterone, and imbalance in estrogen to progesterone ratio are assumed among its causes, as well. Furthermore, many women associate the onset and resolution of cyclical mastalgia with a hormonal event, such as pregnancy or taking the oral contraceptive pill .
In contrast, there is no relationship to the menstrual cycle with non-cyclical mastalgia. Non-cyclic breast pain may result from pregnancy, mastitis, trauma, thrombophlebitis, macrocysts, psychologic disturbance, benign tumors, or cancer. However, only a minority of breast pain is explained by these conditions. Most non-cyclic breast pain arises for unknown reasons. Typically, it presents at a later age; most women are in the fourth or fifth decade of life at diagnosis. Many women are postmenopausal at onset of symptoms. Unfortunately, the course of both cyclical and non-cyclical mastalgia may be long and last many years.
The origin of extra-mammary pain is variable. Referred pain from cardiac, pulmonary and gastrointestinal causes, such as angina, pneumonia and oesophagitis, respectively, need to be excluded. A common cause of extra-mammary mastalgia arises from inflammation of the costochondral junctions of the chest wall (Tietze's disease). This condition usually resolves with rest and non-steroidal anti-inflammatory drugs .
Mastalgia may be bilateral, may be in only one breast or part of one breast, and may radiate to the axilla and down the medial aspect of the upper arm. The affected breast is often extremely tender to touch and pain may be accompanied by swelling and congestion.
A variety of medical therapies such as non-steroidal anti-inflammatory drugs (NSAIDs), vitamin B2, B6, E and C, diuretics, progesterone, thyroxin, Tamoxifen, Bromocriptine, Danazol, and plant extracts like evening primrose oil (EPO) and vitexagnus castus have been recommended for treatment of mastalgia. Unfortunately, Non-cyclic mastalgia responds poorly to medical treatment.
Psychological reassurance and active life style play a role to decrease the pain and low-fat, high-carbohydrate diet can also effect an improvement.
the female breast supplied its innervation from the anterior and lateral cutaneous branches of the second to the sixth intercostal nerves .
Tamoxifen is one of the medical treatment of mastalgia and considered as a first medication line. Tamoxifen 10 mg daily is effective in the treatment of mastalgia. It has side effects commonly observed in short-term treatment as weight gain, nausea, hot flashes (10%), bloating (5% or less), menstrual irregularity, amenorrhea (10%) and vaginal dryness. Thromboembolic is a rare but serious side effects of tamoxifen so it is contraindicated in women with a history of thromboembolic disease.
Pulsed radiofrequency (PRF) has recently been developed with widely usage by pain practitioners as alternative therapeutic technique for relief of chronic pain .
In our study, the investigators aim that the additional pulsed radiofrequency of 2nd , 3rd and 4th thoracic dorsal root ganglia to the routine regimen treatment of mastalgia tamoxifen 10 mg daily may improve breast pain severity and quality of life.
Our proposal: Is to find that pulsed radiofrequency of 2nd , 3rd and 4th thoracic dorsal root ganglia may improve breast pain severity and quality of life.
Aim of the work: This study aimed to evaluate the efficacy of additional pulsed radiofrequency (2nd , 3rd and 4th thoracic dorsal root ganglia) to the routine regimen treatment of mastalgia tamoxifen 10 mg daily.
Hypothesis: Management of non cyclic mastalgia is a challenging issue needing more appropriate method to reach the best result.
Recharge Gap: To our knowledge, there is a no researches discuss this issue and how to manage it in best way.
Patients and methods:
After approval of the local ethics committee (Mansoura university), twenty six patients complain from non-cyclic mastalgia aged from 18 to 60 with VAS > 4 was enrolled in this prospective study who were recruited from outpatient pain clinic in Oncology Center Mansoura University.
Sample size:
It was assessed using G-power analysis. Assuming α (type I error) = 0.05 and β (type II error) = 0.2 (power = 80 %) and effect size (δ) = 0.6 yielded a total sample size of 26.
Patients was randomly classified into two groups:
Group A (n=13): they was received Tamoxifen 10 mg daily. Group B (n=13): they was received Tamoxifen 10 mg daily and pulsed radiofrequency of 2nd , 3rd and 4th thoracic dorsal root ganglia.
Exclusion criteria: cyclical mastalgia, extra-mammary mastalgia patients refusal, suspicion of malignancy, acute inflammatory breast conditions, presence of polycystic ovarian diseases or cervical hyperplasia, pregnant patients and patients during lactation period, coagulopathy disorder, sepsis at the side of injection, history of thromboembolic disease, mental disorder and who was not willing or cannot finish the whole study, disturbed anatomy (congenital, traumatic, and postsurgical), which increase the intervention difficulty.
All patients in group B will inform about the procedure and its possible consequences. Written informed consent was obtained from all patients before the procedure.
Technique:
An intravenous cannula was inserted and secured. All suitable resuscitation equipment and drugs will available. Vital signs, heart rate, blood pressure and oxygen saturation will monitored throughout the procedure and up to 1 hour after the block performance.
Resuscitation equipment must be readily available including endotracheal tubes of different sizes, ambu bag, ventilator, druges eg. atropine and adrenaline.
The procedures were performed on a 64 MDCT scanner (Brilliance 64-Philips). The CT acquisition parameters were 200 mAs, 120 kVp, 512 × 512 matrix, 1.172 pitches, 64 × 0.625 mm section collimation, and 4 mm slice thickness.
Patients were lying prone. First, a level of T2, 3, 4 disc was detected then the target 2nd, 3rd and 4th thoracic nerve roots were identified. After marking the entry points, adequate sterilization of the skin was achieved using bovidone iodine then the skin was anasthesied by 2 ml lidocaine 2% at each entry point. The Baileys radio frequency (RF) 22G, 10 cm, sharp needles with 10 mm active tip was introduced to face the 2nd, 3rd and 4th thoracic nerve roots. If the lung or the pleura are within the needle path injection of saline in order to push the lung or the pleura away from the field.
When confirm the place of the needles tips, the sensory and motor stimulations were done by the RF generator to get sensory paresthesia along T2, T3 and T4 dermatomes at 0.4-0.8 V and intercostal fasciculation were obtained at double the sensory amplitude.
The PRF course was carried out at 42°C for 120 s twice at each level followed by injection of 1 ml lidocaine 2% and 1 ml dexamethasone 4 mg at each level.
After intervention, All patients were transferred to a recovery room for observation and record any complication.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Tamoxifen group | Other | Drug: Tamoxifenthey was received Tamoxifen 10 mg daily. |
| Tamoxifen and pulsed radiofrequency group | Active comparator | Other: pulsed radiofrequency of 2nd , 3rd and 4th thoracic dorsal root ganglia., Drug: Tamoxifenthey was received Tamoxifen 10 mg daily and pulsed radiofrequency of 2nd , 3rd and 4th thoracic dorsal root ganglia. |
Who may qualify
- Ages
- 20 to 60 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (1 listed)
- complain from non-cyclic mastalgia aged from 20 to 60 with VAS > 4
Key exclusion criteria (12 listed)
- cyclical mastalgia
- extra-mammary mastalgia
- patients refusal
- suspicion of malignancy
- acute inflammatory breast conditions
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 |
|---|---|---|
| pulsed radiofrequency of 2nd , 3rd and 4th thoracic dorsal root ganglia.Patients were lying prone. Firstly, T2, 3, 4 disc level was detected then the target 2nd, 3rd and 4th thoracic nerve roots were identified. After marking the entry points, adequate sterilization of the skin was achieved using bovidone iodine then the skin was anasthesied by 2 ml lidocaine 2% at each entry point. The Baileys radio frequency (RF) 22G, 10 cm, sharp needles with 10 mm active tip was introduced to face the 2nd, 3rd and 4th thoracic nerve roots.The PRF course was carried out at 42°C for 120 s twice at each level followed by injection of 1 ml lidocaine 2% and 1 ml dexamethasone 4 mg at each level. | Other | Tamoxifen and pulsed radiofrequency group |
| Tamoxifenreceived Tamoxifen 10 mg daily | Drug | Tamoxifen and pulsed radiofrequency group, Tamoxifen group |
Primary outcome
VAS
Time frame: 3 months
0=no pain, 10=worst pain
2 secondary outcomes
Immediate complications for ex
Time frame: one day
Side effect of Tamoxifen
Time frame: 3 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 7 Mar 2019.
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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 2 study testing pulsed radiofrequency of 2nd , 3rd and 4th thoracic dorsal root ganglia. and Tamoxifen in people with Breast Fibroadenoma, run by Mansoura 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 1 inclusion and 12 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 7 Mar 2019. 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.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
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?
VAS (time frame: 3 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 7 Mar 2019.