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Effect of Laser Acupoints on Fallopian Tube Obstruction

Effect of Laser Acupoints on Fallopian Tube Obstruction

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07351747
Enrollment
36
Registered
2026-01-20
Start date
2025-04-01
Completion date
2026-04-01
Last updated
2026-01-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acupoints, Fallopian Tube Obstruction, Laser

Brief summary

This study aims to determine the efficacy of laser acupoint therapy on treating fallopian tube obstruction.

Detailed description

Fallopian tube obstruction is a significant health concern that affects a substantial number of women worldwide, often leading to infertility and other reproductive issues. The fallopian tubes, essential components of the female reproductive system, play a crucial role in the process of conception by facilitating the transport of ova from the ovaries to the uterus. The laser's focused light energy, when directed at specific acupoints linked to reproductive health, is hypothesized to activate the body's energy pathways or meridians, thereby facilitating healing and restoration of normal tubal function. Although acupoint therapy shows promise, laser acupoint therapy offers potential advantages over traditional acupuncture by utilizing low-level lasers, which may enhance the treatment's efficacy. Laser acupoint therapy is noninvasive and painless, making it articularly appealing for patients who have a fear of needles or are sensitive to pain.

Interventions

OTHERLaser acupoints therapy + Standard care

Patients will receive laser acupoints therapy addition to standard care.

OTHERStandard care

Patients will receive placebo laser acupoints therapy in addition to standard care.

Sponsors

Kafrelsheikh University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* Women aged 20-35 years - nulliparous. * Women diagnosed with fallopian tube obstruction. * Body mass index less than 30 kg/m2. * Consent to participate in the study. * General good health with no major co-existing medical conditions that could interfere with the treatment or outcomes. * No prior fertility treatments \[e.g., In vitro fertilization (IVF), intrauterine insemination (IUI)\] within the last 6 months. * Ability to attend all scheduled sessions and follow-up assessments.

Exclusion criteria

* Currently pregnant or breastfeeding. * History of pelvic surgery within the past year. * Presence of severe systemic diseases such as active cancer or severe cardiovascular diseases. * History of allergic reactions or adverse responses to acupuncture or laser therapies. * Currently undergoing hormonal therapy or use of hormonal contraceptives. * Current or recent history of genital tract infections, including sexually transmitted. infections, which could affect the reproductive system. * Presence of significant uterine anomalies diagnosed through imaging that could impact fertility. * Polycystic Ovary Syndrome (PCOS).

Design outcomes

Primary

MeasureTime frameDescription
Tubal patency3 months post-treatmentHysterosalpingography (HSG) will be used to assess tubal patency. It is a radiographic technique where a contrast material is injected into the uterine cavity, and X-ray images are taken to evaluate the shape of the uterus and the status of the fallopian tubes. HSG will be applied before the treatment and again three months post-treatment to evaluate changes in tubal patency HSG will be applied before treatment and after 3 months post-treatment.

Secondary

MeasureTime frameDescription
Anti-Müllerian Hormone (AMH) Test3 months post-treatmentA blood test will be used to measure the level of Anti-Müllerian Hormone (AMH), which is an indicator of the remaining quantity of eggs and ovarian function. This test will be conducted before the treatment and at the third month of treatment to monitor any changes in ovarian reserve.
Quantitative Pregnancy Test3 months post-treatmentA blood test that will be measured the specific level of Human Chorionic Gonadotropin (hCG), which is produced during pregnancy. This test will be performed every month.

Countries

Egypt

Contacts

CONTACTHadeer E Shalaby, MBBCH
hadeershaalaaby@yahoo.com00201554488336

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026