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Levonorgestrel-releasing Intrauterine System and Tubal Ligation

Levonorgestrel-releasing Intrauterine System: A Emerging Tool for Conservative Treatment of Pain and Bleeding After Tubal Ligation

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04663568
Enrollment
2
Registered
2020-12-11
Start date
2020-12-01
Completion date
2021-12-01
Last updated
2022-11-30

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

Conditions

Tubal Ligation

Brief summary

Today tubal sterilization is a simple, safe, and cost-effective method of achieving long-term contraception. Sterilization is an ideal method of permanent contraception in developing countries where access to health care providers is limited. The percentage of women who use sterilization as a method of contraception rises from about 5% between 20 and 24 years of age to almost 50% for those between 40 and 44 years of age. The most widely touted and most significant health benefit of tubal sterilization appears to be a reduced risk of ovarian cancer. Post-tubal ligation syndrome includes pain during intercourse, aching lower back, premenstrual tension syndrome, uterine hemorrhage, and absence of menstruation. The syndrome is caused by blood circulation problems in and around the Fallopian tubes and ovaries, pressure on nerves, and intrapelvic adhesion. Since the symptoms of this syndrome are mild, simple symptomatic treatment is sufficient in most cases. In some cases, however, hysterectomy may be necessary.

Interventions

Levonorgestrel-releasing intrauterine system will be inserted during the menstrual cycle

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
30 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* Women aged from 30-40 year * Woman subjected to tubal ligation * Women 12 month postpartum * Non lactating women * Nomedical disorders

Exclusion criteria

* contraindication for Levonorgestrel-releasing Intrauterine System * Women with any uterine or ovarian pathology * women refuse to participate

Design outcomes

Primary

MeasureTime frameDescription
The level of pain from before to 6 months after levonorgestrel-releasing intrauterine system insertion6 monthsvisual analogue scale from 0 (minimum value) to 10 (maximum value)

Countries

Egypt

Outcome results

None listed

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