Clinical Trials Directory

Trials / Terminated

TerminatedNCT04663568

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
Phase
N/A
Study type
Interventional
Enrollment
2 (actual)
Sponsor
Assiut University · Academic / Other
Sex
Female
Age
30 Years – 45 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DEVICELevonorgestrel-releasing intrauterine systemLevonorgestrel-releasing intrauterine system will be inserted during the menstrual cycle

Timeline

Start date
2020-12-01
Primary completion
2021-12-01
Completion
2021-12-01
First posted
2020-12-11
Last updated
2022-11-30

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04663568. Inclusion in this directory is not an endorsement.