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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.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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.

Egypt1 site
  • Yahay wahba

    Al Mansurah

Other trials in Egypt

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.

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 groups in NCT03715413
Study groupRoleWhat they receive
Tamoxifen groupOtherthey was received Tamoxifen 10 mg daily.
Receives: Drug: Tamoxifen
Tamoxifen and pulsed radiofrequency groupActive comparatorthey 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.

  1. VAS

    0=no pain, 10=worst pain

    Measured: 3 months

Secondary outcomes (2)
  1. Immediate complications for ex

    Hematoma, neurological deficits or respiratory insufficiency (dyspnea or pneumothorax).

    Measured: one day

  2. 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.

  1. First posted23 Oct 2018
  2. Study start15 Aug 2018
  3. Primary completion1 Dec 2018
  4. Study completion1 Dec 2018

Resources

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)
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

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.

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