Effect of anaesthetic spray in addition to local injectable anaesthesia as pain relief for scrapping the inner layer of uterus
- Conditions
- Diseases of the genitourinary system, (2) ICD-10 Condition: O||Medical and Surgical,
- Registration Number
- CTRI/2021/01/030835
- Brief Summary
Patients fulfilling the eligibilty criteria will be included after obtaining informed consent. Detailed history, clinical examination and routine preoperative investigation will be done and patients will be allocated into group 1 and group 2.In Group 1 patients 10ml of 1% lignocaine will be injected paracervically at 5 and 7 o’ clock at the junction of cervix and vagina for Paracervical block(PCB). In Group 2 patients,3 puffs of lignocaine spray(30mg of 10% lignocaine) will be directed on cervix and vaginal vault. After a waiting period of 2 minutes cervix will be held with an instrument and another 3 puffs will be directed towards the cervical external os. After further waiting period of 2 minutes 10ml of lignocaine will be injected paracervically at 5 and 7 o’clock at the junction of cervix and vagina for PCB .After PCB patients will undergo uterine curettage procedures according to the institution protocol. Pain score will be qualified by numeric pain rating scale(NPRS) which will be explained to the patient before the procedure. NPRS will be used after holding the cervix, immediately after the procedure,30 minutes and 1 hour after the procedure.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Female
- Target Recruitment
- 100
Patients planned for uterine curettage procedure under paracervical block.
Hypersensitivity to lignocaine Active genital tract infection Past history of cervical surgery History of chronic pelvic pain.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the effect of lignocaine spray plus paracervical block with paracervical block alone for pain relief by Till 1 hour post procedure immediately after procedure Till 1 hour post procedure after holding the cervix with instrument Till 1 hour post procedure 30 minutes post procedure Till 1 hour post procedure 1 hour post procedure Till 1 hour post procedure
- Secondary Outcome Measures
Name Time Method Side effects between the 2 groups Compare satisfaction score between the 2 groups using 5 point likert scale
Trial Locations
- Locations (1)
Department of obstetrics and gynecology
🇮🇳Pondicherry, PONDICHERRY, India
Department of obstetrics and gynecology🇮🇳Pondicherry, PONDICHERRY, IndiaDr RamalakshmiPrincipal investigator9629162506padma95lakshmi@gmail.com
