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Effect of Oral Tramadol Administration Prior to IUD Insertion

Safety and Efficacy of Oral Tramadol Administration in Reducing Pain During Levonorgestrel Intrauterine Device Insertion in Adolescents and Young Women: a Randomized Controlled Trial

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04312061
Enrollment
108
Registered
2020-03-18
Start date
2020-03-30
Completion date
2020-07-05
Last updated
2020-03-18

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

Conditions

Contraception

Brief summary

the aim of the study is to evaluate the safety and efficacy of oral tramadol administration in reducing pain during LNG- IUD insertion in adolescents and young women

Interventions

oral tramadol tablet 5o mg given 1 hour before LNG-IUD insertion

DRUGPlacebo oral tablet

oral placebo tablet given 1 hour before LNG-IUD insertion

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
14 Years to 25 Years
Healthy volunteers
No

Inclusion criteria

* nulliparous adolescents and young women requesting LNG-IUD insertion

Exclusion criteria

* parous women, contraindications to LNG-IUD insertion and allergy or contraindications to tramadol

Design outcomes

Primary

MeasureTime frameDescription
pain during IUD insertion5 minutesintensity of patient-perceived pain at time of IUD insertion, using a visual analog scale. The VAS scale is graded from 0 to 10 on a 10 cm horizontal straight line, where 'zero' corresponds to no pain at all, and '10' to the worst possible pain imaginable.

Secondary

MeasureTime frameDescription
duration of the procedure5 minutesduration of IUD insertion from speculum in to speculum out in minutes

Contacts

Primary ContactAHMED SAMY
ahmedsamy8233@gmail.com+201100681167

Outcome results

None listed

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