Clinical and radiographic success of pulpotomy in primary molars restored with glass ionomer- crown

Evaluation of clinical and radiographic success of pulpotomy in primary molars restored with glass ionomer- crown: A double-blind randomized clinical trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT201609226105N6

Enrollment

Registered

2016-11-14

Start date

2016-12-29

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

Dental Caries. Other and unspecified infectious diseases

Interventions

Intervention 1: Intervention 1 Applying topical anesthesia gel (TOPEX, Sultan Healthcare IND. CO, USA) for 60 seconds, administration mandibular block anesthesia by delivering 1 mL of lidocaine 2% wit

Intervention 1 Applying topical anesthesia gel (TOPEX, Sultan Healthcare IND. CO, USA) for 60 seconds, administration mandibular block anesthesia by delivering 1 mL of lidocaine 2% with epinephrine 1

?????? 2 ????? ?? ?? ??? ????? (TOPEX, Sultan Healthcare IND. CO, USA) ?? ??? 60 ?????? ????? ?? ??? ???? ?????? ?? ????? 1 ???? ???? ?? ????? ????????? 2% ?? ??? ????? 80000/1 (Persocaine-E, Darou P

Eligibility

Sex/Gender

All

Age

4 Years to 8 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria :Children between 4-8 years old, require pulpotomy in the primary mandibular second molars, having complete physical and mental health, located in the positive or definitely positive classification of Frankle during behavioral pretreatment assessment, existence of enough crown tissue to repair, nearly the same crown destruction on molars of both sides . Exclusion criteria :Any known allergy to medication or anesthetic solution, any emergency situation or tooth pain with pulp-origin .

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Clinical success. Timepoint: 6 months after intervention 1 and 2. Method of measurement: using described criteria of successful clinical treatment including no swelling, tenderness to percussion, tenderness to palpation, mobility, fistula and abscess.	—

Secondary

Measure	Time frame
Radiographic success. Timepoint: 6 months after intervention 1 and 2. Method of measurement: using described criteria of successful radiographic treatment including no PDL widening, loss of lamina dura, radiolucency of furcation, internal or external root resorption, supporting bone destruction, pre apical radiolucency.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNahid Ramazani

Zahedan University of Medical Sciences

ramazani_nahid@yahoo.com+98 54 3341 4005

Outcome results

None listed

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