Skip to content

Effect of single drug in premenstrual problem

Efficacy of Qust in Premenstrual Syndrome-A randomized controlled study

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/03/012328
Enrollment
60
Registered
2018-03-05
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- PREMENSTRUAL SYNDROME

Interventions

Intervention1: Qust: Fine Powder of Qust 3gm orally in capsules form ( 3 cap. twice a day) Control Intervention1: Sumbul-ut-teeb: Fine powder of Sumbul-ut-teeb 3gm orally in capsule form ( 3 cap. twi

Sponsors

National Institute of Unani Medicine
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with regular cycle and a cycle length of 21- 35 days presenting with signs and symptoms of premenstrual syndrome Symptoms only during the premenstrual period with marked relief at onset of menstruation PMTS-O with VAS scale

Exclusion criteria

Exclusion criteria: Patients on hormonal replacement therapy, oral contraceptive, undergone hysterectomy Diagnosed cases of pschyiatric disorder, lactating mother Present with any organic pelvic pathology, irregular menstrual cycle Patients with any systemic and metabolic diseases

Design outcomes

Primary

MeasureTime frame
Patient presenting with â?¥1 of the following symptoms. Depression, irritability, anxiety, angry outburst, confusion, social withdrawal, breast tenderness, abdominal bloating and pain , headache, swelling of extremities Timepoint: 15 days prior to expected date of mentruation for 2 cycles

Secondary

MeasureTime frame
Premenstrual tension scale- self rating with VAS scale(PMTS-SR with VAS)12, SF-12 SCORE Timepoint: 15 days prior to expected date of mentruation for 2 cycles

Countries

India

Contacts

Public ContactDr Wajeeha Begum

Rajiv Gandhi University of Health and Sciences

drwajeehanium@gmail.com9972550185

Outcome results

None listed

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