Comparison of the administration time of diclofenac suppository on post-operative pain in transvaginal oocyte retrieval under general anesthesia in infertile women

Comparison of the administration time of diclofenac suppository on post-operative pain in transvaginal oocyte retrieval under general anesthesia in infertile women: a double-blind randomized clinical trial

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT20120215009014N259

Enrollment

Registered

2019-01-24

Start date

2018-06-22

Completion date

Unknown

Last updated

2019-02-25

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

Conditions

Female infertility. Female infertility

Interventions

Intervention 1: Intervention group: Diclofenac suppository 100 mg single dose 15 minutes before transvaginal oocyte retrieval under general anesthesia. Intervention 2: Control group: Diclofenac suppos

Eligibility

Sex/Gender

Female

Age

18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Age of 18 to 45 years; Infertile women candidate for IVF

Exclusion criteria

Exclusion criteria: A previous history of IVF; Number of follicles less than two; Using NSAIDS or alcohol; Sensitivity to diclofenac; Psychological problems; A history of convulsion; Chronic disease such as hepatitis, renal failure, cardiovascular, peptic ulcer, inflammatory bowel disease

Design outcomes

Primary

Measure	Time frame
Assessing the pain. Timepoint: At 15, 30, 60, and 120 minutes after operation. Method of measurement: Using visual analog scale (VAS).	—

Secondary

Measure	Time frame
Assessing the nausea and vomiting. Timepoint: At 15, 30, 60, and 120 minutes after operation. Method of measurement: By physical examination and history taking.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNiloofar Molaei

Hamedan University of Medical Sciences

niloofar.mollaei@gmail.com+98 81 3828 3939

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026