Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
FEMALE
Healthy Volunteers
NCT07326007

Verbal Analgesia Versus Standard Technique for Pain Control During Copper T380A Intrauterine Device Insertion in Women With Previous Cesarean Delivery

Led by Cairo University · Updated on 2026-01-08

88

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Insertion of copper IUDs is often associated with moderate pain, which may reduce acceptance and continuation rates. Factors such as nulliparity and absence of prior vaginal delivery are known to increase pain perception. Women who have delivered only by cesarean section represent a special subgroup because their cervix has not undergone vaginal dilation and cervical remodeling, making insertion technically more difficult and often more painful. This group has been underrepresented in prior analgesia trials, highlighting an important evidence gap.

CONDITIONS

Official Title

Verbal Analgesia Versus Standard Technique for Pain Control During Copper T380A Intrauterine Device Insertion in Women With Previous Cesarean Delivery

Who Can Participate

Age: 18Years - 45Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Women aged 18 to 45 years
  • Desire to use Copper T380A IUD
  • History of delivery only by cesarean section with no vaginal delivery
Not Eligible

You will not qualify if you...

  • Current pelvic infection, cervicitis, or vaginitis
  • Uterine anomalies or fibroids distorting the uterine cavity
  • Contraindication to copper IUD procedure
  • Use of any analgesic medication within 6 to 8 hours before insertion
  • Pregnancy or suspected pregnancy
  • Severe dysmenorrhea requiring narcotic medication

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Al Gezeera Hospital

Giza, Egypt

Actively Recruiting

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Research Team

M

Mahmoud Alalfy

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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