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Assessment of intravenous sedation effect on pain of surgical removing polyps compared with local anesthesia

Assessment of intravenous sedation effect on surgery pain in hysteroscopic polypectomy compared with paracervical block

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016031426855N3
Enrollment
84
Registered
2016-04-28
Start date
2016-04-18
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

polypectomy. Polyp of corpus uteri

Interventions

Intervention 1: General anesthesia: 1 micro grams/ kg Fentanyl and 0.1 mg/kg Midazolam is injected and consequently 100 micro grams / kg Propofol is infused. Then the surgery starts. Intervention 2: I
Treatment - Drugs
General anesthesia: 1 micro grams/ kg Fentanyl and 0.1 mg/kg Midazolam is injected and consequently 100 micro grams / kg Propofol is infused. Then the surgery starts.
In intravenous sedation: 1 micro grams/kg fentanyl and 0.1 mg/kg Midazolam is injected. Then 3 micro grams / kg Propofol is infused.
In paracervical block: 10 cc of 2% Lidocaine is injected in 4 and 8 o'clock of cevicovaginal mucous in Lithotomy position.

Sponsors

Tehran University of Medical Sciences , Deputy of Research
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients aged between 18- 50 years old with polyps less than 3 cm; no history of cardiopulmonary diseases. Exclusion criteria: Lidocaine sensitivity; excess anxiety.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The pain of surgery. Timepoint: During and 3 hours after surgery ( in general anesthetic group: only the pain of 3 hours after surgery). Method of measurement: Visual analogue scale.

Secondary

MeasureTime frame
Post operative recurrence of polyp. Timepoint: 6 months after surgery. Method of measurement: Ultrasound.;Duration of operation. Timepoint: From anesthesia induction to discharge of recovery room. Method of measurement: Hour.;Complications of analgesia method. Timepoint: During analgesia, during surgery and 3 hours after surgery. Method of measurement: Check list.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Razavi

Arash Women's Hospital,Tehran University of Medical Sciences

mrazavi@razi.tums.ac.ir+98 21 7771 9922

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 27, 2026