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Not yet recruiting NCT06755528

Effect of Shockwaves on Fallopian Tubes Adhesion

No phase Interventional Fallopian Tube Adhesion

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Chitosan, shockwave therapy.
Who it may be relevant to
Registry conditions: Fallopian Tube Adhesion. Basic parameters: 25 years — 35 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Effect of Shockwaves on Fallopian Tubes Adhesion: a Randomized Controlled Trial

Overview

The purpose of this study is to determine the effect of shock waves on fallopian tube adhesions.

Detailed description

Tubal factor infertility accounts for approximately 40% of the cases of female infertility. Identifiable causes of tubal infertility are post-infectious tubal damage, endometriosis-related adhesions, and postsurgical adhesion formation.

Although surgical management is considered as a common choice for treating blocked tubes or adhesion it has many complications such as: infection, creation of more scar tissue, damage to organs and bleeding.

Shock waves is a modality that exerts an anti-inflammatory action and regenerative effect as well biological model. Shock waves can be nowadays considered an effective, safe, versatile, repeatable, noninvasive therapy for the treatment of many musculo-skeletal diseases, and for some pathological conditions where regenerative effects are desirable, especially when some other noninvasive/conservative therapies have failed.

For these reasons and complications of surgery, This study aims to examine the effect of shockwaves therapy on fallopian tubes adhesion

Interventions

  • Drug Chitosan
    The participants will receive medications for fallopian tube adhesions (Chitosan (glucosamine (GIcN) and N-acetylglucosamine (GIcNAc) units,1 tablet per day) as prescribed by the gynecologist
  • Device shockwave therapy
    The participants will receive shockwave with the following parameters: sonic pulses characterized by: high peak pressure, up to 100 mpa (500 bar) or even more, rapid rise in pressure (\<10 ns), short duration (\<10 μs) and a broad range of frequency. The energy flux density was 0.09 to 0.16 mJ/mm2; with a frequency of 5 Hz and 2000 impulses, i session per week for 4 weeks.

Primary outcome measures

  • Assessment of Fallopian tube adhesions [Time frame: 4 weeks]
  • Detection of Fallopian tube patency [Time frame: 4 weeks]

Eligibility criteria

Inclusion criteria

  • Their ages will be ranged from 25 to 35 years old.
  • Their body mass index (BMI) will be less than 35kg/m².
  • All women will be diagnosed with fallopian tubes adhesion by the physician.
  • They have regular menstrual cycles.
  • All Patients have secondary infertility and they have previous caesarean section).

Exclusion criteria

  • Any gynecological diseases (uterine prolapse, retroversion flexion of the uterus or chronic pelvic pain).
  • Leukemia or tumor (spinal or pelvic tumor).
  • Diabetes mellitus, hypertension, heart diseases, cardiovascular diseases and skin diseases.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06755528 · P.T.REC/012/003490

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗